Treating tumors using implants comprising combinations of allogeneic cells

ABSTRACT

This invention provides methods and compositions for treating tumors by implanting near the tumor an alloactivated cell population. The cell population is made up of a plurality of third-party donor cells that have been cultured together ex vivo, and harvested near the time of peak cytokine secretion. Once placed in the tumor bed, the alloactivated cells recruit active participation of the host, which then reacts against the tumor and provides a level of ongoing protection. Employing multiple third party donor cells confers particular advantages in terms of effectiveness, timing, and ease of use.

REFERENCE TO RELATED APPLICATION

This application claims the priority benefit of U.S. provisionalapplication Ser. No. 60/061,766, filed Oct. 10, 1997 ABN. The priorityapplication is hereby incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

The present invention relates generally to the fields of cellularimmunology and cancer therapy. More specifically, it relates to thetreatment of tumors or the generation of an anti-tumor immune responseby implanting a mixture of alloactivated allogeneic cells in or aroundthe tumor site.

BACKGROUND

Cancer continues to be a leading cause of mortality around the globe.Traditional regimens of cancer management have been successful in themanagement of a selective group of circulating and slow-growing solidcancers. However, many solid tumors are resistant to traditionalapproaches, and the prognosis in such cases is correspondingly grave.

One example is brain cancer. Each year, approximately 15,000 cases ofhigh grade astrocytomas are diagnosed in the United States. The numberis growing in both pediatric and adult populations. Standard treatmentsinclude cytoreductive surgery followed by radiation therapy orchemotherapy. There is no cure, and virtually all patients ultimatelysuccumb to recurrent or progressive disease. The overall survival forgrade IV astrocytomas (glioblastoma multiforme) is poor, with ˜50% ofpatients dying in the first year after diagnosis. Because these tumorsare aggressive and highly resistant to standard treatments, newtherapies are needed.

Another example is pancreatic cancer, the fifth leading cause ofcancer-related deaths in the United States. The disease is associatedwith a high mortality rate, with a medium survival for untreatedpatients after diagnosis of about 4 months. Ninety percent of pancreaticcancer patients initially present with locally advanced, surgicallyunresectable disease. Current therapy for these patients is strictlypalliative and does not significantly impact on overall patientsurvival. Most recently, the chemotherapeutic agent, Gemcitabine(GEMZAR™) was shown to improve overall median survival to 5.7 monthscompared to that of 5-fluorouracyl (4.2 months) and had a betterclinical benefit index. However, it is clear that even with these neweragents, palliation of the disease is highly temporary.

An emerging area of cancer treatment is immunotherapy. There are anumber of immunological strategies under development, including: 1.Adoptive immunotherapy using stimulated autologous cells of variouskinds; 2. Systemic transfer of allogeneic lymphocytes; 3. Vaccination ata distant site to generate a systemic tumor-specific immune response; 4.Implantation of immune cells directly into the tumor.

The first of these strategies, adoptive immunotherapy, is directedtowards providing the patient with a level of enhanced immunity bystimulating cells ex vivo, and then readministering them to the patient.The cells are histocompatible with the subject, and are generallyobtained from a previous autologous donation.

One version is to stimulate autologous lymphocytes ex vivo withtumor-associated antigen to make them tumor-specific. Zarling et al.(1978) Nature 274:269-71 generated cytotoxic lymphocytes in vitroagainst autologous human leukemia cells. In U.S. Pat. No. 5,192,537,Osband suggests activating a tumor patient's mononuclear cells byculturing them ex vivo in the presence of tumor cell extract and anon-specific activator like phytohemagglutinin or IL-1, and thentreating the culture to deplete suppresser cell activity. Despite theseexperimental observations, systemic administration of ex vivo-stimulatedautologous tumor-specific lymphocytes has not become part of standardcancer therapy.

Autologous lymphocytes and killer cells may also be stimulatednon-specifically. In one example, Fc receptor expressing leukocytes thatcan mediate an antibody-dependent cell-mediated cytotoxicity reactionare generated by culturing with a combination of IL-2 and IFN-γ (U.S.Pat. No. 5,308,626). In another example, peripheral blood-derivedlymphocytes cultured in IL-2 form lymphokine-activated killer (LAK)cells, which are cytolytic towards a wide range of neoplastic cells, butnot normal cells. In combination with high dose IL-2, LAK cells have hadsome success in the treatment of metastatic human melanoma and renalcell carcinoma. Rosenberg (1987) New Engl. J Med. 316:889-897. Forexamples of trials conducted using LAK in the treatment of brain tumors,see Merchant et al. (1988) Cancer 62:665-671 & (1990) J. Neuro-Oncol.8:173-198. While not associated with serious clinical complications,efficacy is typically only anecdotal or transient.

Another form of adoptive therapy using autologous cells has beenproposed based on observations with tumor-infiltrating lymphocytes(TIL). TILs are obtained by collecting lymphocyte populationsinfiltrating into tumors, and culturing them ex vivo with IL-2. TILshave activity and tumor specificity superior to LAK cells, and have beenexperimentally administered, for example, to humans with advancedmelanoma. Rosenberg et al. (1990) New Engl. J. Med. 323:570-578.Unfortunately, TILs can only be prepared in sufficient quantity to beclinically relevant in a limited number of tumor types, and remainexperimental.

The second of the strategies for cancer immunotherapy listed earlier isadoptive transfer of allogeneic lymphocytes. The rationale of thisexperimental strategy is to create a general level of immunestimulation, and thereby overcome the anergy that prevents the host'simmune system from rejecting the tumor. Strausser et al. (1981) J.Immunol. Vol. 127, No. 1 describe the lysis of human solid tumors byautologous cells sensitized in vitro to alloantigens. Zarling et al.(1978) Nature 274:269-71 demonstrated human anti-lymphoma responses invivo following sensitization with allogeneic leukocytes. Kondo et al.(1984) Med Hypotheses 15:241-77 observed objective responses of thisstrategy in 20-30% of patients, and attributed the effect to depletionof suppressor T cells. The studies were performed on patients withdisseminated or circulating disease. Even though these initialexperiments were conducted over a decade ago, the strategy has notgained general acceptance, especially for the treatment of solid tumors.

The third of the immunotherapy strategies listed earlier is thegeneration of an active systemic tumor-specific immune response of hostorigin by administering a vaccine composition at a site distant from thetumor.

Various types of vaccines have been proposed, including isolatedtumor-antigen vaccines and anti-idiotype vaccines. Another approach isto use tumor cells from the subject to be treated, or a derivative ofsuch cells. For review see, Schirrmacher et al. (1995) J Cancer Res.Clin. Oncol. 121:487-489. In U.S. Pat. No. 5,484,596, Hanna Jr. et al.claim a method for treating a resectable carcinoma to prevent recurrenceor metastases, comprising surgically removing the tumor, dispersing thecells with collagenase, irradiating the cells, and vaccinating thepatient with at least three consecutive doses of about 10⁷ cells.

In yet another approach, autologous or syngeneic tumor cells aregenetically altered to produce a costimulatory molecule. For reviewssee, Pardoll et al. (1992) Curr. Opin. Immunol. 4:619-23; Saito et al.(1994) Cancer Res. 54:3516-3520; Vieweg et al.(1994) Cancer Res.54:1760-1765; Gastl et al. (1992) Cancer Res. 52:6229-6236; and WO96/07433. Tumor cells have been genetically altered to produce TNF-α,IL-1, IL-2, IL-3, IL-4, IL-6, IL-7, IL-10, IFN-α, IFN-γ and GM-CSF.

International patent application WO 98/16238 describes cancerimmunotherapy using autologous tumor cells combined with allogeneiccytokine-secreting cells. The vaccines comprise a source oftumor-associated antigen, particularly tumor cells from the patient tobe treated, combined with an allogeneic cytokine-secreting cell line.Exemplary cytokines are IL-4, GM-CSF, IL-2, TNF-α, and M-CSF in thesecreted or membrane-bound form. The cytokine-producing cells provideimmunostimulation in trans to generate a specific immune responseagainst the tumor antigen. Vaccines can be tailored for each type ofcancer or for each subject by mixing tumor antigen with an appropriatenumber of cytokine-producing cells, or with a cocktail of such cellsproducing a plurality of cytokines at a favorable ratio.

The fourth of the immunotherapy strategies listed earlier is intra-tumorimplantation, directed at delivering effector cells directly to the siteof action. The proximity of the effector cells to the target is supposedto promote the ability of the transplanted cells to react with thetumor, generating a graft versus tumor response.

Kruse et al. (Proc. Natl. Acad. Sci USA, 87:9377-9381, 1990) analyzedvarious effector cell populations in adoptive immunotherapy of the 9Lrat gliosarcoma cell line. Different cell populations were prepared thatwere designed to have a direct effector function against the cancercells. Included were syngeneic lymphocytes, nonadherentlymphocyte-activated killer (LAK) cells, adherent LAK cells, syngeneiccytotoxic T lymphocytes (CTL) raised against tumor antigens, andallogeneic CTL raised against alloantigens. The allogeneic cytotoxic Tlymphocytes were claimed to prevent tumor take. The CTL were prepared bycoculturing thoracic duct lymphocytes from one inbred rat strain withspleen cells from rats syngeneic to the challenged animals, underconditions and for a period designed to enrich for cytotoxic effectorcells. Treatment was effected by coinjecting the CTL with the tumorcells into the brains of rats in conjunction with recombinant IL-2, andthen readministering the CTL on two subsequent occasions. The regimenwas claimed to forestall tumor take by 17 days. The authors state thatthe tumor is successful in the brain, because the brain is animmunologically privileged site which prevents the administered cellsfrom being eliminated before they perform their function. A corollary ofthis is that the treatment would not be effective at other sites (suchas the pancreas and the breast) that are not immunologically privileged.

In a subsequent study, Kruse et al. (J. Neuro-Oncol., 19:161-168, 1994)performed intracranial administrations of single or multiple sourceallogeneic cytotoxic T lymphocytes. In this study, the 9L cancer cellline was injected into rats only 6 days before the initiation oftreatment. A series of four injections of allogeneic T lymphocyteswithin the next 17 days was performed, and had the effect of extendingthe median life span of the rats by 19 days (about the same interval asthe treatment protocol). There is no evidence for any lasting effect,despite the fact that four doses of the effector cells are given. Thisis consistent with the author's hypothesis that the tumoricidal effectis generated by the CTL themselves, and disappears once the administeredcells are eliminated.

Two other publications by the same group demonstrates the naturalprogression of this CTL implantation technology in a direction towardsgreater enrichment for cells with a direct effector action against thetumor.

J. M. Redd, et al. Cancer Immunol. Immunother., 34:349, 1992 describe amethod of generating allogeneic tumor-specific cytotoxic T lymphocytes.CTL were generated in culture from an inbred rat strain allogeneic tothe tumor cell line. The cells were found to lyse both tumor cells andCon A stimulated lymphoblasts of the same tissue type. Thetumor-specific subset was deliberately selected and enriched as beingspecific for a determinant expressed only by the tumor. The articleconcludes by stating that the ultimate goal of the authors is totransfer the technology to humans using allogeneic CTL lackingspecificity for normal brain antigens (i.e., depleted of alloreactivecells). This is a significant elucidation of the previous article byKruse et al. in Proc. Natl. Acad. Sci. (supra, p. 9579 col. 1), in whichthey refer to two types of allogeneic CTL, one of which is tumorspecific and one of which is allospecific. The yield of tumor specificcells was substantially lower. The article by Redd et al. teaches thatthe tumor specific cells are preferred, and provides a way of enrichingfor them when using cultured rat cells.

More recently, Kruse et al. (Proc. Am. Assoc. Cancer Res. 36:474, 1995;FASEB J. 10:A1413, 1996) briefly outline a clinical study of human braincancer patients. The patient's lymphocytes were expanded with OKT3 andIL-2, then co-cultured with allogeneic donor cells for 18-21 days in thepresence of IL-2. Such culture conditions would result in a populationhighly enriched for terminally differentiated effector cells. Patientsenrolled in the Phase I study received CTL into the tumor bed and wereplaced with a catheter for subsequent infusions. Ongoing treatmentinvolved 1 to 5 treatment cycles every other month, with each cycleconsisting of 2-3 CTL infusates within a 1 to 2 week period. Again, theongoing necessity to readminister the cells is consistent with theauthor's stated objective of providing cells with a direct cytolyticeffect on the tumor.

The necessity of ongoing repeated administration of the effector cellsto the tumor through a cannula severely limits the practical utility ofthis technology, both in terms of expense and the inconvenience to thepatient.

In view of the limitations of may of these strategies, new approaches tothe treatment of cancer are needed.

Considerable progress was made towards a simpler and more effectiveimmunotherapeutic strategy by the development of cytoimplants. SeeInternational patent application WO 96/29394, a “Method for TreatingTumors”. Potent cellular compositions are placed directly into the tumorbed, leading to beneficial effects for patients with different types ofcancers. The method can be conducted as follows: The tumor patient'sleukocytes are co-cultured in a mixed lymphocyte cell reaction withhealthy lymphocytes derived from an allogeneic donor. The alloactivatedcells are surgically implanted at the tumor site, and produce a mixtureof cytokines which induce a primary immune response. During thisreaction, the host lymphoid cells identify both the graft lymphoid cellsand tumor tissue as foreign.

SUMMARY OF THE INVENTION

The present invention provides compositions and methods for treating atumor or eliciting an anti-tumor immunological response in a humanpatient. The compositions contain a combination of cells that areallogeneic to the subject being treated, at least one of which has beenalloactivated in culture. The compositions are designed for implantationinto the tumor bed of the patient, where they evoke a local reactionwith a long-term beneficial effect on the tumor.

Certain embodiments of the invention relate to methods for preparing apharmaceutical composition containing alloactivated human donorlymphocytes for treating a tumor in a human patient, comprising thesteps of (a) coculturing lymphocytes from a first human donor allogeneicto the patient, and leukocytes from a second human donor allogeneic toboth the first human donor and the patient, so as to alloactivate thelymphocytes; (b) harvesting the cells and preparing them for humanadministration at a time when they are effective in the treatment of thetumor. The alloactivated cells are typically harvested from culture nearthe time of peak cytokine secretion, and are typically effective whengiven as a single dose.

Also embodied are pharmaceutical compositions prepared according to theaforementioned methods, in some forms containing approximately 2×10⁹ to2×10¹⁰ alloactivated cells. The pharmaceutical compositions are suitablefor human use after washing substantially free of substances like growthfactors and serum inappropriate for administration, and in substantiallysterile condition.

Also embodied is a cell population containing lymphocytes from a firsthuman that are alloactivated against leukocytes from a second human, foruse in a method of treatment of a third human by surgery or therapy.Optionally, the cell population contains leukocytes from at least threedifferent humans. The cell populations can be used in a medicament fortreatment of a tumor or raising an anti-tumor immune response in a humanpatient. The medicament is implanted at the site of a solid tumor, withor without prior resection or partial resection.

Also embodied are methods for treating a tumor in a human patient orraising an anti-tumor immune response, comprising implanting in oraround the bed of a solid tumor in the patient a cell populationcomprising alloactivated human lymphocytes, the cell population havingbeen produced by coculturing lymphocytes from a first human donor exvivo with leukocytes from a second human donor allogeneic to both thefirst human donor and the patient. The effect can optionally be boostedby implanting a second alloactivated cell population or administering acellular vaccine.

Potential benefits of administering the compositions of this inventioninclude limiting the extent of tumor growth, improving quality of life,or extending the median life expectancy.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a bar graph showing the effect of different alloactivatedlymphocyte preparations on providing resistance to a secondary challengewith J588L lymphoma cells in Balb/c mice. Allogeneic cells stimulatedeither with syngeneic splenocytes or certain third-party splenocytes areboth effective.

FIG. 2 is a bar graph showing the effect of different cell cultureratios on survival time in the mouse lymphoma model.

FIG. 3 is a bar graph showing the degree of functional activity indifferent human alloactivated cell preparations, as determined in fourdifferent assays.

FIG. 4 is a bar graph showing the level of secretion of the cytokinesIL-2 and IFN-γ by human alloactivated cell preparations.

FIG. 5 is a bar graph showing the enhancement of alloactivation of humanlymphocytes by using a plurality of different stimulator cells.

FIG. 6 is a bar graph showing the degree of functional activity ofdifferent human alloactivated cell preparations, depending on the ratioof responder:stimulator cells.

FIG. 7 is a bar graph showing the effect of including 20 μg/mL ofhistidine (dark shading) or cimetidine (light shading) into cultures ofhuman cells; either the responder alone, the stimulator alone, or mixedcultures at a responder:stimulator ratio of 10:1.

DETAILED DESCRIPTION

This invention provides therapeutic compositions for use in cancertreatment. The compositions contain live cells, and confer a long-termbenefit to human cancer patients when administered into a solid tumormass.

The results of an instructive experiment are shown in FIG. 1. Balb/cmice were treated with a histocompatible lymphoma and an alloactivatedcell population. When the lymphocytes in the population have beenagainst host alloantigens (C57×Balb/c or Aj×Balb/c), a proportion of themice clear the first dose of lymphoma cells. Some surviving mice aresufficiently well protected to survive a second challenge with thelymphoma cells, consistent with ongoing specific immunity against tumorantigens. It has now been discovered that lymphocytes activated againstalloantigens unrelated to those of the treated subject (C57×Aj) are alsoeffective in conferring survival from tumor challenge.

Thus, cells from one donor can be alloactivated against alloantigens asecond donor, and still be effective when administered into the tumorbed in a subject who is unrelated to either donor.

The invention shares several features with the method for treatingtumors described in International Patent Application WO 96/29394. Thelive cells in the composition of the present invention includelymphocytes that are allogeneic to the subject being treated, and whichhave been alloactivated before use in treatment. The cells are implanteddirectly in or around a solid tumor mass in the patient, with or withoutresection or partial resection of the tumor.

A key difference is the alloantigens that the lymphocytes in thecomposition have been activated against. In the WO 96/29394 application,the lymphocytes are activated using leukocytes of the patient to betreated, and are therefore primed specifically against the alloantigensof the patient. In the present invention, the lymphocytes are activatedagainst alloantigens of a second unrelated donor. The donor isinvariably allogeneic to the patient at a number of loci for both classI and class II histocompatibility antigens. As a consequence, thelymphocytes are typically not primed specifically against alloantigensof the intended recipient.

Not all third party responder:stimulator cell combinations are equallyeffective in generating a strong alloreaction. This disclosure providesa number of strategies for overcoming relatively less activecombinations.

One strategy is a number of screening assays to measure the extent ofalloactivation early in culture. These are detailed in Example 3.Preferred cell populations for use in this invention are those that showa high degree of alloactivation within the first three days, as measuredby one or more of the screening assays. This permits various donor:donorcell populations to be screened in advance of use in therapy.

A second strategy is to use a plurality of third party donors as asource of responder cells, stimulator cells, or both. This isillustrated in Example 5. Using a plurality of donors helps ensure thatat least some histoincompatibilities will lead to sufficientalloactivation, as measured in the screening assays. In addition, it hasbeen found that cultures prepared with leukocytes from three or moredonors can achieve higher overall levels of alloactivation.

A third strategy is to include in the alloactivation culture an H2receptor antagonist such as cimetidine. This is also illustrated inExample 5. The use of H2 receptor antagonists brings certain relativelyinactive cell combinations over the threshold to measurablealloactivation, and increases the extent of alloactivation in others.

The present invention confers a number of advantages in comparison withpreviously known technology. For example, it is sometimes is difficultto get enough patient leukocytes to use as stimulators for preparingalloactivated cells. This invention provides that leukocytes fromunrelated healthy donors can be used instead, thereby providing analmost limitless supply. In addition, particular donor combinations thatgenerate high levels of alloactivation can be identified in advance, andused to provide a reliable source of effective material. Alloactivatedcells may be stored or produced on an ongoing basis, eliminating thenecessity of withholding treatment for the two to three days necessaryto alloactivate lymphocytes using leukocytes of the patient.

A further description of preferred methods to prepare and use thecompositions of this invention are provided in the sections that follow.

DEFINITIONS

“Mixed lymphocyte reaction”, “mixed lymphocyte culture”, “MLR”, and“MLC” are used interchangeably to refer to a mixture comprising aminimum of two different cell populations that are allotypicallydifferent. At least one of the allotypically different cells is alymphocyte. The cells are cultured together for a time and undersuitable conditions to result in the stimulation of the lymphocytes. Afrequent objective of an MLC is to provide allogeneic stimulation suchas may initiate proliferation of the lymphocytes; but unless indicated,proliferation during the culture is not required. In the proper context,these terms may alternatively refer to a mixture of cells derived fromsuch a culture. When cells from an MLC are administered as a bolus to ahuman, especially in a tumor bed, it is referred to as a “cytoimplant”.

The terms “vaccine”, “immunogen”, or “immunogenic composition” are usedherein to refer to a compound or composition, as appropriate, that iscapable of either: a) generating an immune response against an antigen(such as a tumor antigen) in a naive individual; or b) reconstituting,boosting, or maintaining an immune response in an individual. Theimmunological response may comprise antibodies, immunoreactive cells(such as helper/inducer or cytotoxic cells), or any combination thereof,and is preferably directed towards an antigen that is present on a tumortowards which the treatment is directed.

A “cell line” or “cell culture” denotes higher eukaryotic cells grown ormaintained in vitro. It is understood that the descendants of a cell maynot be completely identical (either morphologically, genotypically, orphenotypically) to the parent cell.

“Inactivation” of a cell is used herein to indicate that the cell hasbeen rendered incapable of cell division to form progeny. The cell maynonetheless be capable of response to stimulus, or biosynthesis and/orsecretion of cell products such as cytokines. Methods of inactivationare known in the art. Preferred methods of inactivation are treatmentwith toxins such as mitomycin C, or irradiation. Cells that have beenfixed or permeabilized and are incapable of division are also examplesof inactivated cells.

The term “cancer cell”, used either in the singular or plural form,refer to cells that have undergone a malignant transformation that makesthem pathological to the host organism. Primary cancer cells (that is,cells obtained from near the site of malignant transformation) can bereadily distinguished from non-cancerous cells by well-establishedtechniques, particularly histological examination. The definition of acancer cell, as used herein, includes not only a primary cancer cell,but any cell derived from a cancer cell ancestor. This includesmetastasized cancer cells, and in vitro cultures and cell lines derivedfrom cancer cells.

The term “tumor-associated antigen” or “TAA” refers to a molecule,complex, or epitope that is detected at a higher frequency or density bytumor cells than by non-tumor cells of the same tissue type. Knowledgeof the existence or characteristics of a particular tumor-associatedantigen target is not necessary for the practice of the invention.

As used herein, “treatment” refers to clinical intervention in anattempt to alter the natural course of the individual or cell beingtreated, and may be performed either for prophylaxis or during thecourse of clinical pathology. Desirable effects include preventingoccurrence or recurrence of disease, alleviation of symptoms,diminishment of any direct or indirect pathological consequences of thedisease, preventing metastasis, lowering the rate of diseaseprogression, amelioration or palliation of the disease state, andremission or improved prognosis.

The “pathology” associated with a disease condition is anything thatcompromises the well-being, normal physiology, or quality of life of theaffected individual. This may involve (but is not limited to)destructive invasion of affected tissues into previously unaffectedareas, growth at the expense of normal tissue function, irregular orsuppressed biological activity, aggravation or suppression of aninflammatory or immunological response, increased susceptibility toother pathogenic organisms or agents, and undesirable clinical symptomssuch as pain, fever, nausea, fatigue, mood alterations, and such otherfeatures as may be determined by an attending physician.

An “effective amount” is an amount sufficient to effect a beneficial ordesired clinical result, particularly the generation of an immuneresponse, or noticeable improvement in clinical condition. Animmunogenic amount is an amount sufficient in the subject group beingtreated (either diseased or not) sufficient to elicit an immunologicalresponse, which may comprise either a humoral response, a cellularresponse, or both. In terms of clinical response for subjects bearing aneoplastic disease, an effective amount is amount sufficient topalliate, ameliorate, stabilize, reverse or slow progression of thedisease, or otherwise reduce pathological consequences of the disease.An effective amount may be given in single or divided doses. Preferredquantities and cell ratios for use in an effective amount are givenelsewhere in this disclosure.

An “individual” or “subject” is a vertebrate, preferably a mammal, morepreferably a human. Non-human mammals include, but are not limited to,farm animals, sport animals, and pets.

GENERAL TECHNIQUES

The practice of the present invention will employ, unless otherwiseindicated, conventional techniques of molecular biology, microbiology,cell biology, biochemistry and immunology, which are within the skill ofthe art. Such techniques are explained fully in the literature, such as,“Molecular Cloning: A Laboratory Manual”, second edition (Sambrook etal., 1989); “Oligonucleotide Synthesis” (M. J. Gait, ed., 1984); “AnimalCell Culture” (R. I. Freshney, ed., 1987); “Methods in Enzymology”(Academic Press, Inc.); “Handbook of Experimental Immunology” (D. M.Weir & C. C. Blackwell, eds.); “Gene Transfer Vectors for MammalianCells” (J. M. Miller & M. P. Calos, eds., 1987); “Current Protocols inMolecular Biology” (F. M. Ausubel et al., eds., 1987); “PCR: ThePolymerase Chain Reaction”, (Mullis et al., eds., 1994); “CurrentProtocols in Immunology” (J. E. Coligan et al., eds., 1991). See alsoGately et al., Lee et al., and Zarling et al. (infra) for examples oftechniques in mixed lymphocyte cultures.

General procedures for the preparation and administration ofpharmaceutical compositions are outlined in Remington's PharmaceuticalSciences 18th Edition (1990), E. W. Martin ed., Mack Publishing Co., Pa.

There are a number of animal models for cancer that can be used to testand adjust the compositions and methods of this invention, if desired.Certain models involve injecting in-bred animals with establishedsyngeneic tumor lines. The tumors can be co-injected with a potentiallytherapeutic composition, allowed to establish before therapy iscommenced, or administered as a challenge at some time followingvaccination of a naive animal. Illustrations are provided in the Examplesection. Also usefull are chimeric animal models, described in U.S. Pat.Nos. 5,663,481, 5,602,305 and 5,476,993; EP application 379,554; andInternational application WO 91/01760.

All patents, patent applications, articles and publications mentionedherein, both supra and infra, are hereby incorporated herein byreference.

PREPARATION OF ALLOACTIVATED CELL POPULATIONS

The cellular compositions of this invention are prepared byalloactivating one or more responder cell populations containinglymphocytes with one or more stimulator cell populations expressingalloantigens. The source of the responder and stimulator cells areallogeneic both to each other, and to the patient to be treated with theresultant composition.

Source of Donor Cells

The cells that are used to prepare the composition are typically takenfrom healthy unrelated human donors allogeneic to the subject to betreated.

Cells are generally described as allogeneic if they are from the samespecies but bear a phenotypic difference sufficient to stimulate analloreaction. In the context of this disclosure, use of the term“allogeneic” is restricted to a difference in phenotype of majorhistocompatibility complex (MHC) antigens. Any qualitative difference inthe identity of MHC allotypes between cells of the same species meansthey are allogeneic cells. In humans, differences at any of the HLA-A,B, C, D, DP, DQ, and DR loci constitute allotypic differences relevantfor this invention. Identity of HLA-A, B, C, DP, DQ, and DR aretypically determined using allotype-specific antibodies in acytotoxicity or immunofluorescence technique.

Preferred allotypic differences for the purposes of the presentinvention relate to HLA class II antigens. Comparing the class IIantigens of the DP, DQ, and DR loci between the putative allogeneiccells and cells of the subject to be treated, preferably at least 1, andincreasingly more preferably 2, 3, 4, 5, or even 6 loci are differentbetween allogeneic cells. Class II antigens may also be determined atthe D locus by mixed lymphocyte reaction using typed cells. Donors ofallogeneic cells are generally unrelated to the subject being treated,to maximize the number of MHC mismatches. In a normal outbredpopulation, unrelated individuals will almost invariably differ at anumber of different loci.

The number of class II region mismatches is related but secondary to afunctional determination of allogenicity. Allogeneic cells areparticularly suitable for use in the present invention if theydemonstrate a strong proliferative response when tested in alloreactivecultures. Donors of cells previously known or empirically shown toproduce a particularly strong response are especially suitable for usein therapy. As described elsewhere in this disclosure, a panel ofdifferent allogeneic cells can be tested in combinations to determinethose that elicit the strongest degree of alloactivation.

The “responder” cells are capable of specifically reacting to anallogeneic stimulus. The cell population generally contains lymphocytecells or cells of the lymphocyte lineage, particularly T cells.Lymphocytes expressing CD4 antigen (CD4+ cells), and cells expressingCD8 antigen (CD8+ cells) are both included in the definition of Tlymphocytes, and either or both may be included in the composition.Generally, the responder cells are leukocytes obtained from peripheralblood, typically enriched for mononuclear cells (PBMC), and optionallyfurther enriched for cells of the lymphocyte lineage. Particularenriched populations contain at least 10% CD4+ cells or 10%helper/inducer cells; more preferably they are at least about 20% ofCD4+ or helper/inducer cells; even more preferably the portion is atleast about 30% of CD4+ or helper/inducer cells. CD4+ cells may beconveniently quantified with commercially available specific antibodysuch as OKT4 in conjunction with fluorescence-activated counting.However, standard peripheral blood mononuclear cell preparations aresuitably enriched for many applications of this invention. Assays fordetermining the extent of alloactivation are described in the nextsection.

The “stimulator” cells are allogeneic to the responder cells and capableof eliciting an alloreaction in the responders. Suitable cell types foruse as stimulator cells are those that bear a high density of allogeneichistocompatibility antigens, particularly class II antigens. Any type ofcell (not limited to blood cells) bearing sufficient alloantigens can beused. A particularly suitable source is peripheral blood leukocytes orwhite cells. It is desirable to enrich for, or at least not to depletecells expressing class II histocompatibility antigens from thepopulation, such as B cells and monocytes. Extensive subfractionation ofthe cells is not usually required, and a simple peripheral bloodmononuclear cell population (PBMC) is adequate for most purposes.

The combined cell population is not necessarily restricted to one sourcefor the responder cells and one source for the stimulator cells. Two,three, for, or a higher plurality donors may optionally be used tofacilitate collection of the allogeneic cells, to increase stimulationof the allogeneic cells, to minimize the elicitation of an anti-allotyperesponse, or to otherwise enhance the therapeutic efficacy.

Collection and Preparation of Donor Cells

Donors are typically prescreened to identify those with sufficientleukocyte count, and exclude those with neoplastic conditions ortransmissible infections. Collection may be performed by whole blooddonation followed by separation of blood cell populations, or byleukapheresis. Leukapheresis is especially appropriate for collectingthe responder cell population, because the number of cells required issubstantial. Sufficient blood is processed to obtain about 100-500 mLleukapheresis suspension, preferably at least about 200 mL. For example,leukapheresis may be performed using a Cobe 2997 (COBE SPECTRAL®,Lakewood CO); Fenwall CS 300 (Fenwall, Deerfield Ill.); or Haemonetrics(Braintree Mass.) blood cell separator. Flow rates of ˜40-50 mL/min for2-4 h yield ˜200-250 mL leukapheresis suspension having <1 mL red cells,with variations between individual donors and the equipment used.

The collected leukocytes are generally washed to remove platelets, andresuspended in a suitable medium, such as AIM V supplemented with 2%inactivated fetal calf serum. Separation of PBMC and other enrichmentprocedures include centrifugation over a suitable medium such as FICOLL™or HISTOPAQUE®, passage over a nylon-wool column, affinity separationmethods such as panning, or sorting in a fluorescent cell sorter usingan antibody against a relevant cell-surface marker. Where possible, itis generally preferable to decrease the number of manipulation steps.For example, better leukapheresis separation may obviate the need forsubsequent separation on FICOLL™.

Mixed Lymphocyte Cultures

Responder and stimulator cells are combined in a suitable culturemedium, typically supplemented with fetal calf serum or a serumsubstitute, and optionally including other growth factors. The ratio ofresponder:stimulator cells is preferably between about 100:1 to 1:10;more preferably about 50:1 to 1:1; still more preferably about 20:1 to5:1, and even more preferably about 10:1. Where there are a plurality ofstimulator or responder cells in a one-way MLC, the same approximateratio of responders:stimulators is maintained. Thus, when using 2inactivated stimulators, the ratio may be approximately 9:(1:1); whenusing 3 inactivated stimulators, the ratio may be approximately8:(1:1:1). Similarly, when using multiple responders, the ratio may be(5:5):1 or (3:3:3):1. If cultured together, the multiple respondercomposition becomes a multi-way MLC. One-way activation of multipleresponders can be achieved by conducting a separate culture for eachresponder population at a 10:1 ratio, and then combining thealloactivated cells just before use.

This invention encompasses the use of two-way or multi-way mixedlymphocyte cultures, wherein a plurality of cell populations act as bothresponders and stimulators. In certain embodiments of the invention,one-way MLCs are performed by inactivating the stimulator cells, forexample, by treating ˜10⁷ cells/nL with 50 μg/mL mitomycin C orsublethal irradiation, followed by washing.

Once combined in the desired ratio, the cells cultured at an appropriatedensity in a suitable atmosphere (such as 95% O₂, 5% CO₂ at about 37°C.). The culture period is preferably at least about 12 h, morepreferably between about 24 h and 72 h. Additional stimulation may beobtained by culturing for 3-5 days, although this is generally notpreferred, since cytokine levels are normally higher during the first 48to 72 h of culture.

The recitation within this disclosure of preferred cell sources, cellratios, culture conditions, timing, and other features, is intended asan aid to the practitioner and is not meant to limit the scope of theinvention, unless explicitly required. No limitation is implied withrespect to any of the individual parameters, since various otherparameter combinations will generate a cell population with the desiredfunctional effect.

Measuring Functional Criteria of the Alloactivated Cell Population

Once the culture is initiated but before use in therapy, the functionalactivity of the culture can be determined using one or more functionalassays.

Since cytokine secretion is believed to play an important role ineliciting the response in the treated subject, cytokines can be testedin a standard immunoassay. Particular cytokines of interest are IL-2,IL-4, IL-6, TNF-α, LT, IFN-γ, G-CSF, M-CSF (both membrane and secretedform), and GM-CSF. For example, particular degrees of stimulation isindicated by levels of biological activity of TNF-αor LT at 50-150 U/mL,or 500-3500 pg/ml.

Proxies for functional activity of the alloactivated cells include: I:MTT Formazan Reduction Assay; II: XTT Formazan Reduction Assay; III:Flow Cytometry for CD3/CD69 or CD3/FDA; IV: FDA Plate Assay; V: AcidProduction Assay, VI: Acridine Orange Assay. These assays are detailedin Example 3. More traditionally, alloactivation can be determined bycell proliferation, measured by culturing a test sample for 5 days andconducting a standard [³H]-thymidine uptake assay, or by counting blastcells. The predictive value of functional assays can be determined bycomparing results of the assays on cultured cells with the effect of thecells in a suitable animal model. See Example 4.

Preferred cultures are those that show a level of activation ≧10% aboveunstimulated donor control value within one of the first 3 days ofculture, as measured by the Tetrazolium Reduction Assay (XTT), theAcridine Orange Assay (AO) or by Flow Cytometry (CD69), more preferablyattaining the threshold in several of these assays in combination.

Optimizing the Functional Effect

Experience in animal model experiments shows that not all third-partydonors provide the same degree of alloactivation when third party donorare used for both the stimulator and responder cells.

To the extent that variability is donor-cell dependent, donors can bechosen according to experience, both in terms of the degree ofalloactivation observed in culture, and the clinical result. Functionalcriteria indicating a particular level of activation, such as theTetrazolium Reduction Assay (XTT), Flow Cytometry Assay, or the level ofsecretion of certain lymphokines determined by ELISA, may besufficiently predictive of outcome, depending on clinical experience.Once successful donors are identified, they can be constituted in apanel of regular donors sourced by the service lab providing theimmunogenic compositions.

To the extent that the variability depends on the match between donorsand patient, several other selection criteria can also be used. Sincethe efficacy of certain donot-patient combinations may migrate accordingto histocompatibility, donors can be selected, if desired, on the basisof tissue match. Donors of particular human histocompatibility types canbe tested for efficacy with particular tumors, if desired, using one ofthe chimeric animal models listed earlier. A more immediate donoridentification test can be conducted using PBLs from the patient and PBLfrom a selection of potential donors in an in vitro assay. One suchassay is a reverse functional test. In this assay, patients cells areset up in a mixed lymphocyte culture as the responder, using thepotential donor of the alloactivated cells as the inactivatedstimulator.

Since the response is thought to involve cytokine secretion by thealloactivated cells, an alternative predictor may be a two-stageculture. In this approach, a responder:stimulator culture is set upusing the same responder and stimulator cells being tested for use inthe preparative culture. At 3 days, the culture is inactivated withmitomycin or sub-lethal irradiation, so that cells can still producecytokines but not replicate. Leukocytes from the patient are then added,and their response is followed by a functional assay, cytokinesecretion, or T cell proliferation. In a variation of this approach,inactivated tumor cells are also provided in the second stage of theculture, and read-out is determined at the end of the second stage bymeasuring cytolysis of ⁵¹Cr labeled tumor cells.

These assays are described for the benefit of the reader who may wish tooptimize the compositions of this invention in various ways,particularly in setting up a donor panel enriched for high responders.It should be emphasized that the invention can be practiced withoutemploying all of these screening procedures.

As an alternative or in addition to pretesting theresponder:stimulator:recipient combination, the degree of alloactivationor the potential therapeutic outcome can be enhanced by employing eitherof the following strategies: a) using a plurality of donor cells as theresponder or stimulator in the MLC; and/or b) adding an H2 receptorantagonist to the culture medium of the MLC.

Using a plurality of donors for the responder or stimulator cellpopulation confers a number of advantages. It is predicted that therewill be a normalizing effect—when there is a variety ofalloincompatibilities present, there is a stronger possibility that atleast one stimulator cell will stimulate at least one responder cell,and in turn, that at least one responder cell will stimulate the treatedsubject. It is also more convenient, in that the same mixed populationwill be suitable for a variety of patients. Thus, a large batch of mixedalloactivated cells can be prepared and stored frozen, for dispensationon demand. It has also been discovered that having a plurality ofdifferent stimulators can achieve levels of alloactivation higher thanone of the stimulators alone. This is illustrated in Example 4.

Adding an H2 receptor antagonist to the culture medium also has anenhancing effect on alloactivation during the first three days ofculture. This is illustrated in Example 5. Without intending to be boundby theory, it is hypothesized that the H2 receptor antagonist inhibitsthe activity of suppressor T cells in the culture. Thus, it isespecially effective in restoring alloactivation to cell combinationsthat are clearly incompatible, but show little reactivity in a standardMLC. A preferred H2 receptor antagonist is cimetidine, added to theculture medium at between 5 μg/mL and 100 μg/mL, typically 20 μg/mL.

USE OF CELLULAR COMPOSITIONS IN CANCER TREATMENT

The compositions of this invention can be administered to subjects,especially human subjects. They are particularly useful for eliciting animmune response against a tumor-associated antigen, or for treatingcancer.

Objectives of Treatment

One purpose of implanting the cellular compositions of this invention isto elicit an immune response. The immune response may include eitherhumoral or cellular components, or both. Humoral immunity can bedetermined by a standard immunoassay for antibody levels in a serumsample from the treated individual.

Since cellular immunity is thought to play an important role in immunesurveillance of cancer, generating a cellular immune response isfrequently a particular objective of treatment. As used herein, a“cellular immune response” is a response that involves T cells, and canbe observed in vitro or in vivo.

A general cellular immune response can be measured as the T cellproliferative activity in cells (particularly PBL) sampled from thesubject after administration. Inactivated tumor cells, preferablyderived from the subject, are used as stimulators A non-specific mitogensuch as PHA serves as a positive control; incubation with an unrelatedstimulator cell serves as a negative control. After incubation of thePBMCs with the stimulators for an appropriate period (typically 5 days),[³H]thymidine incorporation is measured. If desired, determination ofwhich subset of T cells is proliferating can be performed using flowcytometry. T cell cytotoxicity (CTL) can also be measured. In this test,an enriched T cell population from the subject are used as effectors ina standard ⁵¹Cr release assay. Tumor cells are radiolabeled as targetswith about 200 μCi of Na₂ ⁵CrO₄ for 60 minutes at 37° C., followed bywashing. T cells and target cells (˜1×10⁴/well) are then combined atvarious effector-to-target ratios in 96-well, U-bottom plates. Theplates are centrifuged at 100×g for 5 minutes to initiate cell contact,and are incubated for 4-16 hours at 37° C. with 5% CO₂. Release of ⁵¹Cris determined in the supernatant, and compared with targets incubated inthe absence of T cells (negative control) or with 0.1% TRITON™ X-100(positive control).

Another purpose of implanting the cellular compositions of thisinvention is for treatment of a neoplastic disease, particularly cancer.Beneficial effects are typically immunologically mediated or the resultof an inflammatory infiltrate into the injection site and collateraltumors. Evidence of a host response can be shown inter alia byinfiltration of host leukocytes (such as lymphocytes, histiocytes, andother leukocytes) into the tumor site by standard histomorphologyanalysis. The response is preferably an immunological response, whichmay have humoral or cellular components, and preferably includescytotoxic T cell activity. Immunological activity can be measuredsystemically in standard antibody binding immunoassays or cytotoxicityassays on peripheral blood components taken from the treated subject,using tumor cells as targets. Monitoring the effect according to thesemethods is optional, and the recited features need not be positivelydemonstrated in order for the compositions and treatment methods to fallwithin the scope of this invention, except where required.

Suitable Subjects

The compositions of this invention may be used for administration toboth human and non-human vertebrates.

Typically, the subject will either have cancer, or be at substantialrisk of developing cancer. Typical human subjects for therapy comprisetwo groups, which may be distinguished by clinical criteria. Patientswith “advanced disease” or “high tumor burden” are those who bear aclinically measurable tumor. A clinically measurable tumor is one thatcan be detected on the basis of tumor mass (e.g., by palpation, MRI, CATscan, X-ray, or radioscintigraphy; positive biochemical orhistopathological markers on their own are insufficient to identify thispopulation).

A cellular composition for use in this invention is administered topatients with advanced disease with the objective of palliating theircondition. Ideally, reduction in tumor mass occurs as a result, but anyclinical improvement constitutes a benefit. Clinical improvementincludes decreased risk or rate of progression or reduction inpathological consequences of the tumor.

A second group of suitable subjects is known in the art as the “adjuvantgroup”. These are individuals who have had a history of cancer, but havebeen responsive to another mode of therapy. The prior therapy can haveincluded (but is not restricted to) surgical resection, radiotherapy,traditional chemotherapy, and other modes of immunotherapy. As a result,these individuals have no clinically measurable tumor by the definitiongiven above. However, they are suspected of being at risk for recurrenceor progression of the disease, either near the original tumor site, orby metastases. The adjuvant group may be further subdivided intohigh-risk and low-risk individuals. The subdivision is made on the basisof features observed before or after the initial treatment. Thesefeatures are known in the clinical arts, and are suitably defined foreach different cancer. Features typical of high risk subgroups are thosein which the tumor has invaded neighboring tissues, or which showinvolvement of lymph nodes.

A cellular composition for use in this invention is administered topatients in the adjuvant group in order to elicit an anti-cancerresponse primarily as a prophylactic measure against recurrence.Ideally, the composition delays recurrence of the cancer, or morepreferably, reduces the risk of recurrence (i.e., improves the curerate). Such parameters may be determined in comparison with otherpatient populations and other modes of therapy.

Of course, crossovers between these two patient groups occur, and thecellular compositions can be administered at any time that isappropriate. For example, therapy can be conducted before or duringtraditional therapy of a patient with high tumor burden, and continuedafter the tumor becomes clinically undetectable. Therapy may becontinued in a patient who initially fell in the adjuvant group, but isshowing signs of recurrence.

Examples of tumors that can be treated according to this inventioninclude but are not limited to those on the following list. The listincludes sites that are thought to be immune privileged, such as thebrain, and sites that are not immune privileged, such as the pancreas,colon, breast, and prostate.

Brain tumors, such as astrocytoma, oligodendroglioma, ependymoma,medulloblastomas, and PNET (Primitive Neural Ectodermal Tumor);

Pancreatic tumors, such as pancreatic ductal adenocarcinomas.

Lung tumors, such as small and large cell adenocarcinomas, squamous cellcarcinoma, and bronchoalveolarcarcinoma; Colon tumors, such asepithelial adenocarcinoma, and liver metastases of these tumors;

Liver tumors, such as hepatoma, and cholangiocarcinoma;

Breast tumors, such as ductal and lobular adenocarcinoma;

Gynecologic tumors, such as squamous and adenocarcinoma of the uterinecervix, and uterine and ovarian epithelial adenocarcinoma;

Prostate tumors, such as prostatic adenocarcinoma;

Bladder tumors, such as transitional, squamous cell carcinoma;

Tumors of the RES System, such as B and T cell lymphoma (nodular anddiffuse), plasmacytoma and acute and chronic leukemia;

Skin tumors, such as malignant melanoma; and

Soft tissue tumors, such as soft tissue sarcoma and leiomyosarcoma.

The immune status of the individual may be any of the following: Theindividual may be immunologically naive with respect to certaintumor-associated antigens present in the composition, in which case thecompositions may be given to initiate or promote the maturation of ananti-tumor response. The individual may not currently be expressinganti-tumor immunity, but may have immunological memory, particularly Tcell memory relating to a tumor-associated antigen, in which case thecompositions may be given to stimulate a memory response. The individualmay also have active immunity (either humoral or cellular immunity, orboth) to a tumor-associated antigen, in which case the compositions maybe given to maintain, boost, or maturate the response, or recruit otherarms of the immune system. The subject should be at least partlyimmunocompetent, so as to minimize a graft versus host reaction ofpathological scope. However, it is recognized that cancer patients oftenshow a degree of immunosuppression, and this does not necessarilyprevent the use of the compositions of the invention, as long as thecompositions may be given safely and effectively.

Modes of Administration and Dose

The compositions of this invention can be administered to the subject atthe site of any solid tumor. Circulating cancers are treatable so longas there is at least one solid tumor mass. Metastatic sites, affectednodes, and other sites away from the primary neoplasm are suitable, solong as they are accessible and contain sufficient tumor antigen.

If the solid tumor mass is resectable or partly resectable, then thecomposition can be administered at or near the site or in a cavitycreated by the resection. If the tumor is completely removed, however,then it may be preferable to administer the alloactivated cells to ametastatic site to increase the local amount of bystander tumor antigen.The most convenient time to administer the alloactivated cells to aresectable site is during the time of surgery. To keep the cells at thesite until completion of the surgical procedure, it is convenient toadminister the cells in a pharmaceutically compatible artificial gel, orin clotted plasma.

When the solid tumor mass is not resectable, or where less invasiveprocedures are desired, then the composition can be injected at or nearthe tumor site through a needle. For deeper sites, the needle can bepositioned using ultrasound, radioscintigraphy, or some other imagingtechnique, alone or in combination with the use of an appropriate scopeor cannula. Pancreatic tumors are preferably implanted using aninjection needle positioned by an endoscopic ultrasound guidedtechnique, as described by Chang et al., Gastroenterology 112:A346, 1996(abstract). For this application, the cell population is convenientlyadministered when suspended in isotonic saline or a neutral buffer to avolume of about 10 mL.

The dose given is an amount “effective” in bringing about a desiredtherapeutic response, be it the stimulation of an immune response, orthe treatment of cancer as defined elsewhere in this disclosure. For thepharmaceutical compositions of this invention, effective doses typicallyfall within the range of about 10⁸ to 10¹¹ cells, including allogeneicstimulators and responders. Preferably, between about 1×10⁹ to 5×10¹⁰cells are used; more preferably between about 2×10⁹ to 2×10¹⁰. Multipledoses when used in combination to achieve a desired effect each fallwithin the definition of an effective amount.

The various components of the implant composition are present in an“effective combination”, which means that there are sufficient amountsof each of the components for the composition to be effective.Preferably, at least about 10⁸, more preferably between about 1×10⁹ to5×10¹⁰ and; more preferably between about 2×10⁹ to 2×10¹⁰ respondercells are present. Preferably, at least about 10⁷, more preferablybetween about 5×10⁷ to 5×10⁹ and; more preferably between about 1×10⁸ to2×10⁹ stimulator cells are present. Ratios of allogeneic lymphocytes tostimulator leukocytes is generally between 1:1 and 100:1, usuallybetween about 5:1 and about 25:1, and typically about 10:1. However, anynumber of component cells or other constituents may be used, as long asthe composition is effective as a whole. This will also depend cultureconditions and other factors during preparation.

The pharmaceutical compositions of this invention may be givenfollowing, preceding, in lieu of, or in combination with, othertherapies relating to generating an immune response or treating cancerin the subject. For example, the subject may previously or concurrentlybe treated by chemotherapy, radiation therapy, and other forms ofimmunotherapy and adoptive transfer. Where such modalities are used,they are preferably employed in a way or at a time that does notinterfere with the immunogenicity of the compositions of this invention.The subject may also have been administered another vaccine or othercomposition in order to stimulate an immune response. Such alternativecompositions may include tumor antigen vaccines, nucleic acid vaccinesencoding tumor antigens, anti-idiotype vaccines, and other types ofcellular vaccines, including cytokine-expressing tumor cell lines.

Certain embodiments of this invention relate to combination therapies.In one preferred combination therapy, the subject is given anintra-tumor implant of stimulated allogeneic lymphocytes, either before,during, or after treatment at a site distant from the tumor with acomposition comprising stimulated allogeneic lymphocytes and autologoustumor cells. The preparation and use of vaccines of this nature isdescribed in detail in International application WO 98/16238, which ishereby incorporated herein by reference in its entirety. An illustrativeprotocol for this combination therapy is provided in Example 6. In theillustration, the vaccine is given weekly for four weeks following thecytoimplant, to enhance the extent of the anti-tumor response in thehost or the therapeutic effectiveness. The vaccine can also be givenafter intervals of several months in order to replenish the response.Accordingly, certain embodiments of this invention relate toadministering a cytoimplant, and subsequently boosting the therapeuticeffect or immunological response by administering to the patient acomposition comprising alloactivated human lymphocytes allogeneic to thepatient and an inactivated cell population consisting of tumor cellsfrom the patient or progeny thereof.

While the methods and compositions of this invention are generallyeffective when given at a single dose, it may be desirable toreadminister the composition at intervals of 3-6 months, especially forfast-growing tumors that can be injected through a positioned needle.Accordingly, certain embodiments of this invention relate toadministering a cytoimplant, and subsequently boosting the therapeuticeffect or immunological response by implanting in or around the bed of asolid tumor in the patient a second cell population comprisingalloactivated human lymphocytes allogeneic to the patient.

Timing of administration of compositions of this invention is within thejudgment of the managing physician, and depends on the clinicalcondition of the patient, the objectives of treatment, and concurrenttherapies also being administered. Suitable means of immunologicalmonitoring include a one-way MLR using patient's PBL as responders andprimary tumor cells as stimulators. An immunological reaction may alsobe manifest by a delayed inflammatory response at the injection site.Suitable means of monitoring of the tumor are selected depending on thetumor type and characteristics, and may include CT scan, magneticresonance imaging (MRI), radioscintigraphy with a suitable imagingagent, monitoring of circulating tumor marker antigens, and thesubject's clinical response. Additional doses may be given, such as on amonthly or weekly basis, until the desired effect is achieved.Thereafter, and particularly when the immunological or clinical benefitappears to subside, additional booster or maintenance doses may be givenas required.

When multiple cytoimplants or combinations of implants and cellularvaccines are given to the same patient, some attention should be paid tothe possibility that the allogeneic lymphocytes in the vaccine maygenerate an anti-allotype response. The use of a mixture of allogeneiccells from a plurality of donors, and the use of different allogeneiccell populations in each dose, are both strategies that can helpminimize the occurrence of an anti-allotype response.

During the course of therapy, the subject is evaluated on a regularbasis for general side effects such as a febrile response. Side effectsare managed with appropriate supportive clinical care.

The examples presented below are provided as a further guide to apractitioner of ordinary skill in the art, and are not meant to belimiting in any way.

EXAMPLES Example 1

MIXED LYMPHOCYTE CULTURE PROCEDURE.

Collection of Responder PBMC from Unrelated Donor

Peripheral blood mononuclear cells (PBMCs) were collected byleukapheresis from normal healthy donors unrelated to the patient to betreated. Donors were pre-screened to test for complete blood count (CBC)with differential, Hepatitis A, B, and C, VDRL, and HIV-I.

Approximately 150 to 300 ml of leukapheresis suspension containing PBMCwas collected from each donor, using standard blood donation proceduresfor supportive apheresis according to the manufacturers' instructions.The leukapheresis was performed using a Fenwall CS 3000 (Deerfield, EL)blood cell separator. A flow rate of 40 to 50 ml/min for 2 to 4 hourswith lymphocyte yield of 2-4×10⁹ processed a total donor blood volume of7,000 to 12,000 ml to yield 200 to 250 ml of leukapheresis suspensionhaving less than 1 ml of red cells. If a Cobe 2997 blood cell separatorwas used, the centrifuge rate was 5×g, the flow rate was up to 45ml/min, and the collection rate was no more than or equal to 2.5mil/min.

However, if donor pre-absolute lymphocyte counts were in the 0.6×10⁹ to1.0×10⁹ range, as little as 150 ml of leukapheresis product was drawn.Hematocrit for the final product was 3.5%. At least one total bloodvolume was processed for 80% efficiency of lymphocyte collection.

The anticoagulant used was either 2% citrate or a citrate/anticoagulantratio of ACDA—15 ml/citrate—100 ml; ACDB—25 ml/citrate—100 ml; or CPD—14ml/citrate—100 ml. To obtain the utmost product purity, the actual andfinal product from the cell separator was transported as a pureconcentrate of cells in autologous plasma. The cells were not washed,and no albumin was added.

Preparation of Donor Cells

The leukapheresis product was transported to the MC Oncology ResearchLaboratory for the production of allogeneic mixed lymphocyte cells(MLCs) for immunotherapy.

Cells were drained from the leukapheresis pack into two or three 250 mlcentrifuge tubes, removing and setting aside 3 ml for sterility tests tobe done during centrifugation. Cell concentrate was diluted withphosphate buffered saline (PBS) and centrifuged for 7 minutes at 2,000rpm. Centrifugation was repeated twice for a total of three times towash the cells free of the clotting factor in the donor's serum.

Three 1 ml aliquots from the 3 ml removed from the leukocyte suspensionwere placed into sterile capped tubes for sterility testing. The first 1ml aliquot was added to thioglycollate medium (Difco, Detroit, Mich.)(30-35° C., 48 hr.); a second 1 ml was added to tryptic soy broth(Difco, Detroit, Mich.) (25-30° C., 48 hr.); and the third 1 ml wasadded to RPMI 1640 (GIBCO, Gaithersburg, Md.) with 10% heat inactivatedFBS (RPMI-10%) and 1% L-glutamine, but without antibiotics.

Cells were spin washed twice at 150 g for 10 minutes in PBS to removeplatelets. The supernatant was very carefully discarded as cells were ina slurry and not a pellet. Cells were resuspended in AIM V (GIBCO,Gaithersburg, Md.) supplemented with 2% heat inactivated FBS (2% AIM V)to 420 ml, and placed into a T-175 CM² flask.

Patient or donor blood was diluted 1:1 with sterile saline. For cellseparation, 35 ml of cell suspension was carefully layered onto 15 mlHistopaque® g 1.077 suspension medium (Sigma, St. Louis, Mo.) in each 50ml tube and centrifuged at 250 g for 45 minutes. Centrifugation wasstarted slowly and gradually increased to full speed. Aftercentrifugation, the interface containing mononuclear cells between theHistopaque® suspension medium and the plasma layer was carefullycollected with a 25 ml sterile pipet deposited into clean 50 mlcentrifuge tubes, diluted with 2% AIM V Media 1:1, and centrifuged at550 g for 7 to 10 minutes to form a cell pellet. Cells remained aminimum of time in the Histopaque® suspension medium, because it istoxic to the cells.

The supernatant was discarded, the pellet was resuspended in 2% AIM Vand divided into two 50 ml centrifuge tubes to a total volume 40 ml, andcentrifuged at 550 g for 5 minutes. After washing, the supernatant wasdiscarded. The washing step was repeated twice for a total of threetimes. After the last wash, cells in each tube were resuspended in 50 mlof 2% AIM V. Aliquots of 1 ml of the resuspended cells were diluted to aratio of 1:10 in 2% AIM V per tube, then further diluted 1:1 in TrypanBlue (Sigma, St. Louis, Mo.) to distinguish dead from live cells, andthe live cells were counted in a hemocytometer. Cells were set at2×10⁶/ml with 2% AIM V.

Collection of Stimulator PBMC from Tumor Patients

From 200 to 400 ml of peripheral blood cells were drawn fromglioblastoma patients by vena puncture and placed into 250 ml centrifugetubes, removing and setting aside 3 ml for sterility tests to be doneduring spinning. Blood cells in the centrifuge tubes were diluted withsaline and centrifuged for 7 minutes at 550 g. Centrifugation wasrepeated twice for a total of three times to wash the cells free of theclotting factor in the patient's serum. Sterility testing was conductedas described above.

Cells were washed twice by centrifugation at 150 g for 10 minutes insaline to remove platelets, the supernatant was very carefullydiscarded, and 420 ml of cells were resuspended in a T-175 CM² flask insaline.

15 ml of Histopaque® 1.077 cell separation medium was added to twelve 50ml centrifuge tubes, and 35 ml of cells suspended in saline were layeredonto the Histopaque® 1.077 in each 50 ml tube. The cell suspensions werespun at 250 g for 45 minutes, starting centrifugation slowly andgradually increasing speed.

After centrifugation, the mononuclear cells at the interface between theHistopaque® cell separation medium and the plasma layer were carefullycollected with a 25 sterile pipet into 2 sterile 250 ml centrifuge tubesand diluted with 2% AIM V to a fmal volume of 250 ml. The dilutedmononuclear cells were centrifuged at 550 g for 7 to 10 minutes. Forwashing, the supernatant was discarded, then the cell pellet wasre-suspended with 2% AIM V and centrifuged at 550 g for 5 minutes. Thewashing step was repeated for a total of three times.

After the last washing step, cells were re-suspended in 50 ml of 2% AIMV, 1 ml of the cell suspension was diluted 1:10 in 2% AIM V per tube,and the number of viable cells was determined by enumeration in a 1:1 inTrypan Blue as described above.

It is readily appreciated that this procedure is equally suitable forobtaining stimulator cells from healthy third-party donors.

Alloactivation

The isolated patient PBMCs were re-suspended at 10⁷ cells/ml in AIM V,50 μg Mitomycin C (Bristol-Mayer Squibb, Princeton, N.J.) were added perml of patient cell suspension, and the suspension of PBMCs was incubatedat 37° C. for one hour to block response of the stimulator cells to theresponder cells. After one hour of incubation, the excess mitomycin Cwas washed from the cells by alternate centrifugation (250 g for 5 min),and the cells were resuspended in AIM-V. After mitomycin treatment ofthe patient's PBMCs, the cells were added at a 20:1 to 10:1 donorcell:patient cell ratio to the donor culture).

For co-culture, the donor and mitomycin C-treated patient PBMCsuspension was placed in a sealed sterile Fenwal tissue culture systemespecially designed for culture of PBMC for reimplantation intopatients. Cells were passed in sealed systems via Fenwal cell transferunits and pumps according to the manufacturers instructions, andcultured in a 37° C. incubator for 48 hours.

Sterility Testing of Alloactivated Cells

Two days prior to implantation of the cell suspension, the followingthree sterility tests were performed. 10 ml sterile aliquots wereremoved from each tissue culture bag, placed into sterile capped 15 mlcentrifuge tubes, and centrifuged for 10 minutes at 450 g. In each tube,the pellet was resuspended in 3.0 ml of PBS. A 1 ml aliquot of the cellsuspension was added to each of three sterile capped tubes containing 2ml of thioglycollate broth, tryptic soy broth, or RPMI-10% and incubatedfor 48 hours. Each cell suspension was examined microscopically prior toimplant to detect signs of microbial growth.

On the day of surgery, the cells were centrifuged out of their medium,washed two times with saline and re-suspended in platelet free,decalcified plasma obtained from the patient the previous day. The cellswere transported to the operating room in plasma, then the plasma wasre-calcified by the addition of calciun gluconate so that it clots justbefore implantation into the tumor bed.

The day of surgery a drop of collected cell pellet was again examinedfor sterility under the microscope. Just prior to clotting, a 100μlaliquot of the cell suspension was added to 2 ml each of RPMI-10%without antibiotics, thioglycollate and tryptic soy broth in a sterilecapped tube. The samples were then incubated for four days aftersurgery, and a running log was kept of this last sterility test.

Example 2

CLINICAL TRIAL USING ALLOACTIVATED CELLS IMPLANTED AT THE TUMOR SITES

This experiment confirms that allogeneic cells alloactivated usingpatient leukocytes are effective in cancer treatment.

A Phase I/II clinical trial was conducted to examine the feasibility,tolerability, toxicities and clinical effects associated with a singleintratumoral injection of allogeneic lymphocytes sensitized againstpatient alloantigens. This trial is conducted under the auspices of theappropriate ethical approval committee, and in accordance with aprotocol under the U.S. Food & Drug Administration.

Eligible patients were men and women between 18 and 85 years of age. Atotal of ten patients were studied. Eight patients were enrolled in thetrial, and two additional patients were treated off-study on acompassionate basis. Nine of ten patients had locally advanced,surgically unresectable pancreatic tumors; 40% of the patients had StageII disease, 30% had Stage III disease and 20% had Stage IV disease. Onepatient with Stage I disease was 89 years old, declined surgery and wastreated on a compassionate basis. Seven of ten patients had received noprior therapy, one patient had received prior radiation therapy and twopatients had received prior radiation and chemotherapy.

Preparation of Cells

The procedure for preparing the cytoimplant cells was generally inaccordance with the main features of Example 1. Typically, a volunteerthird-party donor for responder cells is screened by normal blood bankcriteria for suitability. No special matching or identification of HLAtype is performed. Whole blood or leukapheresis is collected from thepatient to be treated; and leukapheresis is collected from the donor onthe same day. Mononuclear cells are prepared from both patient and donorby centrifigation on Ficoll™, and counted to ensure that enough cellsare present to prepare the intended dose. Patient cells are inactivatedby treating for 1 hour with mitomycin C, and then washed.

The cells are combined at a donor:patient ratio of 10:1 to 20:1,depending on the number of patient cells available. The cells aresuspended at 3×10⁶ per mL in AIM 5 medium containing 2% fetal calf serumand antibiotics in a gas-permeable plastic bag, and incubated at 37° C.in an atmosphere of 5% CO₂/95% O₂. No cytokines or other growth factorsare added. After three days, the cells are collected by centrifugationand washed. The cells are then transferred to the clinic in a mediumsuitable for administration. For the treatment of pancreatic cancer, thecells were suspended in a volume of about 10 mL isotonic saline.

Features of the cells are shown on the following table:

TABLE 1 Alloactivated Cells Administered to Humans with PancreaticCancer MLC Total MLC MLC MLC Cell Cell Final Final CD3/** IL-2 INF-γPatient Ratio Dosage Viability Sterility CD69 (ng/mL)+ (ng/mL)+ 001, LM10:1 1.76 × 10⁹* 91% Sterile NA 2779 202 002, SA 10:1 3.5 × 10⁹ 98%Sterile 11.8% 10852  438 003, RW 10:1 2.8 × 10⁹ 88% Sterile NA 2334 383004, OY 20:1 5.9 × 10⁹ 92% Sterile NA 1927  0 005, MR 10:1 6.0 × 10⁹ 95%Sterile NA 3941 298 006, OB 20:1 6.04 × 10⁹  96% Sterile NA  118  0 007,BS 10:1 5.8 × 10⁹ 93% Sterile NA 7307 981 008, LM 10:1 8.9 × 10⁹ 91%Sterile 18.6% 1137 308 009, GS 13:1 10.5 × 10⁹  95% Sterile NA  433  0010, JH 15:1 9.6 × 10⁹ 90% Sterile NA 11858 291

Administration

The treatment was conducted as follows: A sufficient amount of wholeblood or leukapheresis was collected from each patient to prepare thecultured cells used in treatment. The sample was forwarded to theImmunotherapy Lab, and used to prepare stimulator cells for allogeneicstimulation of third-party lymphocytes.

Three days later the cytoimplant cells were administered to the subjecton an out-patient basis. Under light anesthesia, an injection needle waspositioned into the tumor using an endoscopic ultrasound guidedtechnique. The implant cells were rescued from culture, washed,suspended in about 10 mL of injectable isotonic saline, and delivered tothe diagnostic service center. The cells were injected into the tumormass, the device was removed, and the patient was allowed to recover.

Three patients were administered with a single dose of 3×10⁹ implantcells. Four patients were administered with a single dose of 6×10⁹implant cells. Three patients were administered with a single dose of9×10⁹ implant cells.

Follow-up was done one day, one week, one month, and every three monthsafter implantation. Criteria assessed included evidence of toxicity,survival, tumor response (endoscopic ultrasound and/or CT-scan), tumormarkers (CEA/CA19-9) and Karnofsky performance score.

Results

Patients treated with 3×10⁹ cells: Patient 001 was a 78 year old malewith an unresectable clinical Stage IV tumor. The patient receivedtreatment on a compassionate basis, and survived 6.5 months. Patient 002was a 53 year old female with an unresectable Stage III tumor. Thepatient later presented with elevated total bilirubin and died at 4.2months after developing liver metastasis. Patient 003 was a 60 year oldmale with unresectable Stage III tumor. There was a hospital admissionfor synocopal episode. The patient survived 20.8 months.

Patients treated with 6×10⁹ cells: Patient 004 was a 52 year old malewith an unresectable Stage II tumor. The patient was later admitted tohospital with biliary obstruction, cholangitis, and dehydration. Thispatient died 20.7 months after treatment. Patient 005 was an 89 year oldfemale with a Stage I tumor, who was not a candidate for resection dueto her age. She received treatment on a compassionate basis, and died11.3 months later due to myocardial infarction. Patient 006 is a 54 yearold female with an unresectable Stage III tumor. She was later admittedto hospital for intractable nausea, vomiting and dehydration, andsubsequently for gastrointestinal hemorrhage. There was increased tumorsize and liver metastasis. The patient died 4.3 months after treatment.Patient 007 is a 61 year old female with an unresectable Stage II tumor.On follow-up, there was elevated total bilirubin, and the patient wasadmitted with intractable nausea and vomiting, diarrhea, anddehydration, possibly related to colitis flare-up. The patient is stillxalive >13 months after treatment.

Patients treated with 9×10⁹ cells: Patient 008 is a 55 year old femalewith an unresectable Stage IV tumor. No serious adverse events wereobserved, and the patient is still alive >13 months after treatment.Patient 009 is a 54 year old male with an unresectable Stage II tumor.The patient was later admitted for two days for pain and nausea andvomiting. The patient died 11.7 months after treatment. Patient 010 is a68 year old male with an unresectable Stage II tumor. No serious adverseevents were observed, and the patient died 8.5 months after treatment.

Clinical Interpretation

Elevated bilirubin, liver enzymes and nausea/vomiting with dehydrationwere the most common serious adverse events documented which wereconsidered to be due to obstruction of biliary stents. These adverseevents were considered to be associated with the disease rather than thetherapy. Because of its relationship to the timing of the administrationof the cytoimplant, one adverse event (elevated total bilirubin, Grade4) was considered possibly related to therapy. No other serious adverseeffects were observed that were considered to be associated withtherapy.

The median survival for all patients treated in this study was 11.5months (range 4.2 to >21) with a mean survival of greater than 10months. The 6 month, 9 month, and 12 month probability of survival was80% (n=8), 60% (n=6), and 50% (n=5), respectively. The probability ofgreater than eight month survival by dose was 33% for 3×10⁹ cells, 75%for 6×10⁹ cells, and 100% for 9×10⁹ cells. Comparison of mediansurvivals of patients treated with cytoimplant to those treated with5-fluorouracyl (median=4.2 months) or GEMZAR™ (median=5.7 months) wassignificant at p<0.006 and p<0.004, respectively.

Histomorphology

Histology slides were prepared from tissue samples from an 89 year oldfemale diagnosed with pancreatic adenocarcinoma. At the time ofdiagnosis, the tumor was advanced and surgically unresectable. The onlytreatment performed on this patient was the injection of the tumor with6×10⁹ cytoimplant cells. The patient died of a myocardial infarct 11.5months later.

One photomicrograph showed fibrovascular tissue with scatteredindividualized tumor cells. There is a dense lymphocytic and plasma cellinfiltrate. Another field showed lymphocytes rosetting the separatedtumor cells. The tumor cells were dark and shrunken, which is evidenceof apoptosis. Another field showed scattered islands of necrotic tumorcells. There was a very dense infiltrate of lymphocytes, and lymphocytesappear to be trafficking into the site from adjacent venules. In a highmagnification view there was clear evidence of direct contact betweenlymphocytes and necrotic tumor cells.

The histomorphology analysis provide clear evidence of a local responseby cells of the patient after implantation of the alloactivated cells.The data are consistent with the cell response in the patient having adirect role in the beneficial effects of the treatment, as shown bydirect contact between lymphocytes and necrotic tumor cells. To thelimited extent that infiltrating cells are present in untreatedpancreatic cancer, this type of direct contact is not observed.

Example 3

MEASUREMENT OF THE DEGREE OF ALLOACTIVATION

In order to ensure the production of high quality effective MLC cells, amethod of measuring the potency of the alloactivated cells can beemployed. Only cell cultures with activity over and above unstimulatedcontrol cells should be used clinically. It is beneficial to compare theactivity to the unstimulated control, since baseline activity ofmononuclear cells from different individuals varies widely.

Several methods are available for measuring lymphocyte activation.Compared with unstimulated mononuclear cells, alloactivated cells reducemore Formazan dye and have more esterase activity. Turnover of XTT (aFormazan dye) can be easily demonstrated in a 96-well plate bycolorimetric spectrophotometry at 470 nm (reference 650 nm). Activatedcells typically show higher absorbance than controls. Lymphocyteactivation can also be demonstrated by flow cytometric determination ofesterase activity using the esterase substrate, fluorescein diacetate(FDA). T cells with high esterase are not determined using FDA and aPhycoerythrin-labeled CD3 antibody. Esterase activity can be accuratelymeasured in a plate assay by using higher concentrations of FDA anddetermination of esterase activity by spectrophotometry at 494 nm(reference 650 nm) in a 96-well plate format. Background esteraseactivity inherent to serum-containing media is inhibited by addition ofa competitive esterase inhibitor (˜10 mM), arginine methyl ester. Forthe most part, these measures show good correlation with each other andwith blastogenesis.

I: MTT Formazan Reduction Assay

This assay is used to enumerate live cells by ability for culture sampleto reduce MTT to blue-green Formnazan dye, and is also helpful for thedistinguishing activated from inactive cells. It can be used forpractically any cell in practically any media. The usefil cell range isbetween 10⁵ and 5×10⁶ per mL.

Reagents:

96 well plates, flat bottom (not ELISA plates)

5 mg/mL MTT (Sigma) in PBS (frozen)

20% SDS in 45% DMF, 0.2 N HCl (pre-warmed to 37° C.)

Procedure:

Place 100 μL of culture media with cells in 96 well plate in duplicateor triplicate. Use 100 μL of media alone for controls. Leave firstcolumn blank.

Add 10 μL of MTT to each well. Tap plate to mix. Cover plate andincubate 37° C. for 4 hours.

Add 50 μL of SDS solution, avoiding bubbles. Tap to mix. If bubbles arepresent, blow on surface. Count plate at 570 nm (reference 650 nm).

II: XTT Formazan Reduction Assay

This assay is used to enumerate live cells by ability for culture tosample to reduce XTT to red-orange Formazan dye, and is also helpful forthe distinguishing activated from inactive cells. It can be used forpractically any cell in practically any media. The usefull cell range isbetween 10⁵ and 5×10⁶ per mL.

Reagents:

96 well plates, flat bottom (not ELISA plates)

1 mg/mL MTT(2,3-bis(2-methoxy-4-nitro-5-sulfo-phenyl-2H-tetrasolium-5-carboxanilinidesalt, Sigma) in PBS (fresh)

1.53 mg/mL PMS (phenylmethanesulfonyl fluoride, Sigma) in PBS (frozen,protected from light)

Procedure:

Place 100 μL of culture media with cells in 96 well plate in duplicateor triplicate. Use 100 μL of media alone for controls. Leave firstcolumn blank.

Pre-mix PMS with XTT immediately before use (5 μL per mL XTT). Add 50 μLof XTT to each well. Tap plate to mix.

Cover plate and incubate 37° C. for 4 hours. Count plate at 470 nm(reference 650 nm).

III: Flow Cytometry for CD3/CD69 or CD3/FDA

This is a measurement of T lymphocyte activation after mixed lymphocytealloactivation. Activities such as CD69 expression or esterase activitycorrelate with cytokine secretion and can be used as surrogate measuresof lymphocyte activity. Unstimulated lymphocytes do not express surfaceCD69 and have only low levels of non-specific esterases. Once activatedby alloantigens or non-specific mitogens, the expression of CD69 appearswithin 48 hours (peak at 24). Esterase activity increases shortly afterstimulation, and continues for several days. Not all allostimulatedlymphocyte reactions proceed with the same kinetics, and it ispreferable to measure activation on day 1, 2 and 3 of the culture.

Sample:

Test samples of donor and patient cells are mixed in small cultures at0.5×10⁶ cells/mL in 2% FCS-RPMI. These cultures are maintained at 37° C.in 5% CO₂ incubator until testing.

Reagents:

Monoclonal antibodies:

CD3-PE (Coulter)

CD69-FITC (Becton-Dickinson). Keep refrigerated when not in use andprotect from light.

Fluorescein Diacetate (Sigma): Stock solution is prepared at 10 mg/mLDMSO, protected from light, and stored in frozen lot tested aliquots.Make working solution weekly by diluting stock 1:100 in DMSO, keepworking solution refrigerated and protected from light.

D-PBS, 0.5% paraformaldehyde-0.05% TRITON™ X-100 in PBS

Procedure:

Internal control unstimulated and activated mononuclear cells samplesare produced on an as-needed basis. Large lot-tested batches will befrozen in 250 μl aliquots in 10% DMSO freezing media.

Mononuclear cells from a normal donors can be used to produce activatedcontrol specimens. These cells are placed in 2% FCS-RPMI at 0.5×10⁶cells/mL up to 100 mL. Cells are cultured for 2 days at 37° C. in thepresence or absence of 2 μg/mL PHA lectin, or admixed at a ratio of 10:1with a second donor population. The cells are collected bycentrifugation at 350×g for 5 minutes. The media is removed and replacedby {fraction (1/10)}th the volume of DMSO Freezing media, and frozen.When needed, control unstimulated and stimulated cells can be thawedquickly and resuspended at the original volume by adding 9 volumes ofPBS.

Control cells are analyzed according to the protocol below along withsamples from the test culture. The duplicate use of control specimens isan addition quality assurance measure. The percentage of CD69 oresterase positive lymphocytes should be within a 5% variance.

Dilute 5 μL of CD3-PE antibody (per sample) in 0.5 mL PBS (per sample).Add either 10 μL CD69 (per sample) or 1 μL of working solution of FDA(per sample).

To 12×75 mm labeled polystyrene tubes, deliver 0.5 mL of dilutedantibody. Add 100 μL of well mixed sample to each tube, includingreference controls, unstimulated donor cells and the allo-activatedcells. Gently vortex and incubate 30 minutes at room temperature. Add0.5 mL of 0.5% paraformaldehyde-0.05% TRITON™ X-100 PBS and mix.

Counting is performed on an appropriately equipped flow cytometer, suchas the EPICS XL Coulter Flow Cytometer. Histogram 1 (forward scatter vs.CD3) of either protocol should have a generous gate around the CD3+mononuclear cells. Region A should approximate % T-Lymphocytes andshould be passed to Histogram 2. In Histogram 2, the use of side scatterversus CD3 permits discrimination of lymphocytes (low side scatterlevel) from unlysed RBSs, RBC ghosts, platelet aggregates, residualgranulocytes and/or other debris. A gate is drawn around the lymphocytes(see Histogram 2 for example). This second gate is passed to Histogram3, where the CD3+ CD69+ cells or CD3+ FDA+ cells are displayed. Run thecontrol values first to set gates (unstimulated controls). Place thequad stat cursor of Histogram 3 so that the CD69 or FDA high values(Quad 2) are 2%. Leave this gate set when analyzing stimulated samples.

Count at least 5,000 gated cells for each sample to obtain a 97%confidence interval.

IV: FDA Plate Assay

This assay is used to enumerate live cells by ability for culture sampleto turnover the esterase substrate, fluorescein diacetate, and is alsohelpful for the distinguishing activated from inactivated cells. Thisassay can be used for practically any media. The useful cell range isbetween 10⁵ and 5×10⁶ per mL.

Reagents:

96 well plates, flat bottom (not ELISA plates)

10 mg/mL FDA (Sigma) in DMSO (stock, protect from light)

10 mg/mL Arginine methyl ester (Sigma) in DMSO

Procedure:

Place 100 μL of culture media with cells in 96 well plate in duplicateor triplicate. Use 100 μL of media alone for controls.

Make a fresh working solution of FDA by adding 10 μL per mL of PBS ofstock FDA plus 50 μL AME stock per mL. Add 20 μL of FDA working solutionto each well. Tap plate to mix.

Cover plate and incubate 37° C. for 1 hour. Count plate at 494 nm(reference 650 nm).

V: Acid Production Assay

This assay is used to quantitative relative organic acid production incultures. This correlates with the state of activation of cells. Thisassay requires the use of medium containing no more than 2% serum.Practical cell range is 1-5×10⁶ cells/mL incubated from 24-48 hours.

Reagents:

96 well plates, flat bottom (not ELISA plates)

Acid Analysis Reagent. This is made in bulk and stored at 4° C. Add 0.1mg/mL Bromophenol Blue in distilled water. Add sufficient concentratedHCl until the appropriate titration point is met. Titration is performeduntil yellow-green color is obtained after adding 75 μL of reagent to100 μL RPMI 2% FCS in a well of a 96 well plate.

Procedure:

Place 100 μL of culture media with cells in 96 well plate in duplicateor triplicate. Use 100 μL of media alone for controls.

Add 75 μL of Reagent to each well. Tap plate to mix. Count plate at 470nm (reference 650 nm).

VI: Blastogenesis Quantitation

This assay is used to quantitate the absolute number of lymphoblastsproduced in cultures after 7 days. The usefull cell range is between1×10⁵ and 5×10⁶ per mL. Place 1-2 drops of a 7 day culture in a Cytospinchamber and perform Cytospin. Stain dried glass slide with eitherWright's Stain or Diff-Quick Stain. Count number of lymphoblasts andother cells under oil immersion 100X lens of microscope. Count over 300total cells.

In an alternative procedure, spleen cells are cultured in 5×75 mmpolypropylene tubes identical to the AO test. After 7 days at 37° C.,the cells are mixed by vortexing and a cytospin preparation is made(Shandon cytocentrifuge,). The slides are stained with Wright/Giemsastain using an automated slide stainer and the blasts enumeratedmanually by counting at least 300 cells/slide. The percent blasts iscalculated by dividing the number of blasts by the total number ofnucleated cells.

VII: Cell Proliferation Assay

[H³]-Thymidine incorporation into DNA is measured as follows: Responderspleen cells are suspended at 1 million cells/ml in RPMI-1640 containing10% fetal bovine serum, antibiotics (streptomycin/penicillin) and 5×10⁻⁵M 2-Mercaptoethanol. One hundred ul of these cells are seeded intriplicate wells of a u-bottom microtiter plate (Costar). Stimulatorspleen cells are then prepared identical to responder spleen cells butare irradiated with 3000 (Cs¹³⁷ source) prior to use. One hundred ul ofthe stimulator cells are added and the mixed lymphocyte culture isincubated at 37° C. for 7 days in a 95% air/5% CO₂ atmosphere. After 7days 10 ul of H³-thymidine (0.5 mCi/ml, ICN Pharmaceuticals, Costa Mesa,Calif.) is added to each well for 6 hours. The microtiter plate is thenharvested used a MASH harvestor and the amount of incorporated thymidinedetermined by counting the harvested wells in a liquid scintillationcounter. The stimulation index (SI) is then determined by calculatingthe ratio of the CPM of H3-Thymidine incorporated into the MLC culturedivided by the CPM of H3-thymidine incorporated into the control(unstimulated) culture.

VIII: Acridine Orange Incorporation

Potency determination is conducted by incorporation of Acridine Orange(AO): Spleen cells are cultured at 1 million/ml in the same media as thecell proliferation assay but in 5×75 mm polypropylene tubes. Each tubereceives 1 ml of reaction mixture. After 3 to 7 days of incubation at37° C., the tubes are mixed by vortexing, and 200 ul removed and placedin a fresh 5×75 mm polypropylene tube. 50 ul of acridine orange (50mg/ml in PBS) is then added for 15 minutes at room temperature. Thetubes are again mixed by vortexing and the cells analyzed for theincorporation of acridine orange by flow cytometry. Results areexpressed as the ratio of fluorescence intensity of samples of MLCactivated cells versus samples of control (inactivated) cells.

Example 4

ANIMAL MODELING OF IMPLANT THERAPY

Efficacy of Alloactivated Cells Prepared using Third-party Stimulators

Cell compositions were prepared, composed of either unstimulatedallogeneic cells alone, allo-activated syngeneic cells, syn-activatedallogeneic cells or alloactivated allogeneic cells (two separateallogeneic cells), or all-activated allogeneic cells (two separateallogeneic donors). Splenocytes form the mice were used to produce thealloactivated cells by culturing at a ratio of 10:1 responder:stimulatorcells. Splenocyte combinations were cultured in RPMI plus 10% fetal calfserum (FCS) supplemented with penicillin-streptomycin at 3×10⁶/mL at 37°C. for 3 days.

1×10⁶ live J588L lymphoma cells were admixed with 10×10⁶ cultured mousesplenocytes, and then injected into the subcutaneous tissue over theright flank of Balb/c mice. Treated mice were watched for tumor growthfor 3 weeks.

Mice without tumor were rechallenged 1 month later with 1×10⁶ livelymphoma cells alone by left flank subcutaneous injections, and watchedfor tumor growth.

FIG. 1 shows the results of these experiments. The presence of activatedallogeneic cells correlates with a subsequent in vivo antitumor hostresponse. Cell populations prepared using two donors allogeneic to thetreated animal could be used in place of syngeneic or autologous cellsin order to induce an antitumor response. However, not all combinationsof activated allogeneic Donor:Donor cell populations were equallyeffective.

Effect of Ratio of Responder:Stimulator Cells on Efficacy

Cell populations were prepared composed of allogeneic cells activated bya variable number of syngeneic stimulator cells, using C57 splenocytesas the responder and Balb/c splenocytes as the stimulator. The cellswere admixed with live lymphoma cells (J588L cells) and injected intothe flanks of Balb/c mice. Treated mice were watched for tumor growthfor 3 weeks.

FIG. 2 shows the percentage of mice without tumors after primary tumorchallenge (6 mice per group). A lower cell ratio may on some occasionsbe better at inducing an antitumor response in mice.

Impact of Using Splenocytes from Tumor-Bearing Mice on the AntitumorEffect

Splenocytes were taken from naive C57 or Balb/c mice or from a mousebearing a 1 cm lymphoma in the right flank. The cells were cultured for3 days either alone or after admixture with Balb/c cells at a 10:1 ratioat a concentration of 0.5×10⁶ cells/mL in RPMI-10% FCS. Lymphocyteactivation was judged by analyzing the percentage of CD3+/Esterase highpopulation by Flow Cytometry. The percent FDA positive cells was 3.5%using stimulators from healthy Balb/c donors, but only ˜2.5% usingstimulators from tumor-bearing donors.

The cell populations alloactivated with stimulators either from naiveBalb/c mice or from mice bearing J588L tumors were admixed with livelymphoma cells (J588L cells) and injected into the flanks of naiveBalb/c mice. The mice were monitored for tumor growth for 3 weeks. Micewithout tumors were next rechallenged with 1×10⁶ live lymphoma cellsalone in the left flank, and watched for tumor growth. Percent micewithout tumors after secondary tumor challenge was between 30 and 40% inboth groups, being slightly higher in the group treated with cellsstimulated using naive Balb/c donors.

This indicates that cells obtained from healthy donors are equallyeffective as stimulators as cells obtained from animals bearing thetarget tumor.

Resistance of Mice Immunized with Alloactivated Lymphocytes andIrradiated Tumor Cells to Subsequent Tumor Challenge

This experiment tested the immunogenic effect of a cell vaccinecontaining alloactivated lymphocytes mixed with inactivated tumor cells.

C57/BL6 mice (3 per group) were injected subcutaneously with 10⁶irradiated B16 melanoma cells alone, mixed with 10⁷ Balb/c×C57alloactivated lymphocytes, or mixed with 10⁶ IL-4 secreting J588Llymphoma cells (allogeneic to C57). The alloactivated cells wereprepared by culturing Balb/c splenocytes with C57 splenocytes at aration of 10:1 at 3×10⁶/mL in RPMI 10% FCS for 3 days.

Cells were washed in PBS, and injected subcutaneously in the flanks ofnaive C57 mice. After 3 weeks, the mice were rechallenged with 5×10⁵ B16live melanoma cells subcutaneously in the opposite flank. Mice wereobserved for tumor formation and sacrificed after tumors reached 1 cm indiameter.

The mice treated with the alloactivated cells survived significantlylonger than the other groups. The two longest surviving mice finallydeveloped cone-shaped tumors, both of which ulcerated. No other micedeveloped ulcers. Two days after the ulcers appeared, both mice expired.Necropsy of these mice revealed the presence of extremely necrotic tumorcells, with evidence of recent tumor cell lysis in the form of massiveDNA deposition. This necrosis was accompanied by an inflammatoryinfiltrate, consisting mostly of lymphocytes. No other form of infectionwas observed anywhere in the body. No lung metastases were seen. This isin contrast to the large number of lung metastases in control miceharboring B16 melanoma tumors in the flank. Bilateral kidneys in bothmice showed extensive glomerulonephritis, suggesting death from tumorlysis syndrome. No other mice demonstrated these changes.

These results are consistent with the mice treated with thealloactivated cell vaccine developing a specific response that causedmassive lysis of the live cancer cells given in the subsequentchallenge.

In another experiment using a different tumor model, C57/BL6 mice (3 pergroup) were injected subcutaneously with 10⁶ Lewis Lung carcinoma cellsalone, mixed with 10⁷ Balb/c×C57 alloactivated lymphocytes cells, ormixed with 10⁶ IL-4 secreting J588L lymphoma cells (allogeneic to C57).The alloactivated cells were prepared by culturing Balb/c splenocyteswith C57 splenocytes at a ratio of 10:1 at 3×10⁶/mL in RPMI 10% FCS for3 days. All cells were washed in PBS and injected subcutaneously in theflanks of naive C57 mice. Mice were observed for tumor formation, andsacrificed after tumors reached 1 cm in diameter. Mice treated with IL-4secreting cells survived significantly longer than the other groups with2 out of 3 long term survivors. The group treated with alloactivatedcells alone had no long term survivors.

Correlation of Functional Markers with Antitumor Effect

To determine the correlation between in vitro functional assay resultsand potential therapeutic benefit, cultures showing various degrees ofactivation are tested in the mouse lymphoma treatment model. Mixedlymphocyte cultures are set up using splenocytes from a variety ofinbred mouse strains at a 10:1 responder:stimulator cell ratio.Alternatively, cultures are set up using a particularresponder:stimulator strain combination, but at different cell ratios.After three days of culture, the activity is measured in XTT Formazanassay and esterase assay.

Just before injection, the cultured cells are supplemented withadditional splenocytes, as necessary, to normalize the cell ratio, andadmixed with 1×10⁶ live or irradiated J588L lymphoma cells. Thepreparation is the injected into Balb/c mice, and the effect on survivalis monitored. The mice can be rechallenged with a subsequent dose oflive lymphoma cells to test for a persisting immunological response. Thesurvival data is then correlated with the functional activity measuredduring the culture period.

Effect of Alloactivated Cell Composition on Antitumor Effect

As described elsewhere in this disclosure, histamine impairsalloactivation during the lymphocyte culture, as measured in thefunctional assays. Cimetidine, which is an H2 receptor antagonist,promotes alloactivation. In this study, alloactivation cultures areprepared in the presence or absence of 20 μg/mL histidine or cimetidine,tested in the XTT Formazan and esterase assays, and then injected intoBalb/c mice with J588L lymphoma cells to correlate with efficacy.

In another study, the effect of having a plurality of differentstimulator or responder cells is tested. Standard cultures containingC57:Balb/c splenocytes (10:1) are compared for efficacy in the mouselymphoma model with cultures containing: a) C57:Aj:Balb/c splenocytes(9:1:1 or 5:5:1); b) C57:Aj:C3H splenocytes (9:1:1 or 5:5:1); c)C57:Aj:C3H:Balb/c splenocytes (8:1:1:1 or 3:3:3:1).

Example 5

EXPERIMENTS WITH CULTURED HUMAN CELLS

Criteria for Functionality of Alloactivated Cells

The degree of alloactivation (a potential reflection of potency intherapy) can be measured according to the functional assays detailed inExample 3. This example illustrates the degree of activation revealed bythe assays.

Human peripheral blood monocytes were isolated from samples taken from anumber of unrelated human volunteers, and set up in one-way mixedlymphocyte cultures at a 10:1 responder:stimulator ratio as describedelsewhere in this disclosure. The assays were run after 2-3 days inculture.

The results are shown in FIGS. 3 and 4. Each of the individuals isindicated by a unique letter, with the responder cells being indicatedbefore the stimulator cells. Thus, the designation A×B means that cellsfrom individual A were cultured with inactivated cells from individualB.

Compared with unstimulated mononuclear cells, alloactivated cells havemore esterase activity and reduce more XTT (a Formazan dye). Esteraseactivity can also be measured by flow cytometry using the esterasesubstrate, fluorescein diacetate (FDA). T cells with high esteraseactivity can be identified by Phycoerythrin-labeled CD3 antibody inconjunction with FDA. These measures correlate well with blastogenesis(determined after culturing for one week), or the level of IL-2 or IFN-γin the supernatant.

Impact of Using Multiple Allogeneic Stimulator Cells

Allo-activated human lymphocyte cultures were produced using cells fromeither one, two, three or four unrelated donors. 3×10⁶ cells/mL werecultured in 2% FCS-RPMI at 37° C. for 2 days. Two-donor populations wereproduced by admixing responder cells with stimulator cells at a 10:1ratio. Populations containing three or four donor cells were produced bymixing responder cells with two or three different stimulator cells atratios of 9:1:1 or 8:1:1:1.

FIG. 5 shows the characteristics of the cells measured using flowcytometry. All values represent percentage of brightly fluorescent cellsafter counting 4000 cells on a Coulter EPICS XL Cytometer.

The results show that cultures prepared with stimulators from aplurality of donors in certain conditions reach higher levels ofactivation.

Impact of Altering the Ratio of Responder:Stimulator Cells

Mixed lymphocyte cultures composed of allo-activated human peripheralblood mononuclear cells were produced using cells from the same twounrelated donors at ratios of 10:1, 5:1, or 1:1. Cells were cultured at0.5×10⁶ cells/mL in 2% FCS-RPMI for 3 days. The strength of thesecultures was measured using the XTT Formazan reduction assay.

The results are shown in FIG. 6

Impact of Histamine or Cimetidine on Alloactivation

Histamine is known to induce the activity of T suppressor cells. Since Tsuppressor cells can play a role in controlling the activity of the MLR,the effect of histamine and of a potent histamine type 2 (H2) receptorblocking drug, Cimetidine, was tested in alloreacting cell cultures.Cell populations composed of alloactivated human peripheral bloodmononuclear cells were produced using cells from unrelated donors. Allcultures contain a 10:1 ratio of responder:stimulator mononuclear cellsat 0.5×10⁶ cells/mL. In some cultures, 20 μg/mL histamine or 20 μg/mLCimetidine were added on day 0.

FIG. 7 shows the results measured using a Formazan reduction (XTT)assay.

Histamine induced suppression and decreased strength of theallo-activation. Cimetidine enhanced activity, possibly by blocking thedevelopment of suppression.

Example 6

TUMOR REGRESSION ACHIEVED USING STIMULATOR-RESPONDER CELL COMBINATIONSFROM TWO THIRD-PARTY DONORS

This example describes animal experiments in which immunologicaltreatment of established malignant tumors leads to tumor regression andinduction of permanent, long lasting tumor specific immunity.

The tumor used in this study is a non-immunogenic glioma histocompatiblewith the Fischer 344 (F344) rat, designated RT-2 (also known as D74).D74 is an extremely aggressive, transplantable tumor in the F344 ratwith histologic and clinical characteristics of Glioblastoma Multiforme.It is essentially incurable by standard therapeutic protocols.Intracranial implantation of as few as 10 cells results in fatal braintumors in about 40 days. When injected subcutaneously, as few as 500,000cells form progressively growing tumors, first palpable in about 5 days,then progressing to large, 2 to 3 cm tumors in 3 to 4 weeks. D74 is notimmunogenic on its own, as inoculation of naive rats with multiple dosesof large numbers of lethally irradiated (10,000 rads) D74 tumor cellsdoes not confer immunity. Surgical removal of well established growingtumors also does not result in subsequent immunity of the host.

Previous studies had established that cytoimplants are effective both instimulating an anti-cancer immunological response in the treatedsubjects, and providing a significant clinical improvement. Intratumorimplantation of alloactivated cells 10 days after administration of D74cells resulted in a significant slowing of tumor growth, increasingmedian survival from 21 to 31 days. Animals receiving a single implantultimately died of progressive tumor growth. Injection of two successivecytoimplants on Day 10 and Day 17 slowed tumor growth, with 3 out of 5animals showing essentially complete tumor regression. The response inthese animals was found histologically to be accompanied by infiltrationof lymphocytes leading to tumor cell apoptosis and necrosis. Animalsshowing regression of the primary tumors also rejected a D74 parentalchallenge, indicating that systemic immunity to D74 had beenestablished. The reaction was specific, because challenge with thebreast adenocarcinoma line MADB106 led to progressively growing tumors.In another study, animals were treated with two successive cytoimplantsand those not showing complete tumor regression had their tumorsremoved. These animals were also found to be immune to rechallenge withD74 cells in a cell-specific manner.

The current study was designed to test the effect of different donorcell populations in the preparation of the alloactivated cells.

Allogeneic cells were sensitized by in vitro mixed lymphocyte culture(MLC) in the following manner. Spleen cells for use as a source ofresponder or stimulator lymphocytes were aseptically removed and mincedinto single cell suspensions in phosphate-buffered saline (PBS). Thecells were passed through fine mesh gauze to remove small particulatedebris, and washed twice by centrifugation (1500 rpm). The stimulatorcells were inactivated by irradiation with 3000 Rads using a Cs¹³⁷source. Responder cells were cultured at 3 million/mL in RPMI-1640containing 10% fetal calf serum, antibiotics (streptomycin/penicillin)and 5×10⁻⁵ M β-mercaptoethanol; then stimulated with irradiated spleencells at a 5:1 responder:stimulator cell ratio. After 3 days at 37° C.,the cells were harvested by centrifugation, washed twice in PBS, andsuspended in PBS at 500 million/mL. This preparation is referred to inthis example as a cytoimplant.

Cytoimplants were administered to F344 rats bearing established (4 to 7mm) D74 tumors growing in the left thigh. The tumors were initiatedapproximately 10 days earlier by injecting naive F344 ratssubcutaneously with 0.5 million D74 cells suspended in 100 μL PBS.Cytoimplants were suspended in a tuberculin syringe fitted with a 25gauge needle, and were injected directly into the tumor nodule in avolume of about 100 to 250 μL. Tumor sizes were measured bidirectionallyusing calipers 2 to 3 times/week, until the tumors reached 3.0 cm, atwhich time the animals were sacrificed.

The animals received one of several treatment regimens: Group 1 receivedintratumor injections of 250 μL PBS alone on Days 10 and 17 (control,n=4); Group 2 received intratumor injections of 150 million Wistaranti-F344 cytoimplant cells in 250 μL PBS on both Day 10 and Day 17(n=5); Group 3 received intratumor injections of Wistar anti-ACIcytoimplant cells on both Day 10 and Day 17 (n=5); Group 4 received anintratumor injection of Wistar anti-ACI cytoimplant cells on Day 10followed by PVG anti-ACI cytoimplant cells on Day 17 (n=5); Group 5received an intratumor injection of Lewis anti-ACI cytoimplant cells onboth Day 10 and Day 17 (n=5). Thus, Groups 3, 4, and 5 all were treatedwith cytoimplants made with two donor cell populations from differentstrains than the F344 tumor-bearing subjects. The Wistar is an outbredrat strain; the others are inbred. All strains are allogeneic at the MHCin comparison with F344 rats, except for the Lewis strain which issyngeneic.

At Day 23 (six days after the second implant), average tumor diameterswere as follows: Group 1 (saline control): 20 mm (representing growth of˜2 mm per day); Group 2: 10 mm (down from 12.5 mm on Day 20,statistically significant with respect to Group 1); Group 3: 14 mm(statistically significant with respect to Group 1); Group 4: 15 mm(down from 17 mM on Day 21, with at least one animal showing signs ofregression and three showing signs of stabilization); Group 5: 15 mm(with several animals still showing some evidence of tumor progression).

These results show that lymphocytes from a first subject that arealloactivated against leukocytes from a second subject can be used totreat established tumors of a third subject by implantation into thetumor bed. Results in individual subjects treated by the same protocolare heterogeneous. Sequential implants have a synergistic effect, andcan lead to not only extended survival, but also tumor regression.Implant cells work well when they are cultured with stimulator cellsthat are MHC incompatible, and certain donor combinations seem to workbetter than others.

Example 7

CLINICAL TRIALS

This example outlines the testing of implant compositions in conjunctionwith a peripherally administered cellular vaccine composition. Thepreparation and use of MLC tumor vaccines is described in more detail inInternational application WO 98/16238, which is hereby incorporatedherein by reference in its entirety.

All patients are enrolled with informed consent, and randomized into thevarious treatment groups. Tumor cells are obtained during surgicalresection of the primary neoplasm, and cryopreserve at the time ofsurgery. The tumor cells are proliferated ex vivo if necessary to obtainsufficient cells for the anticipated course of therapy. Thawed orcultured tumor cells are subjected to 10,000 rads of gamma irradiation.Preparative-scale mixed lymphocyte cultures using inactivated patientstimulator cells and donor leukocytes are conducted generally asdescribed in Example 1.

The mononuclear cells used to prepare each cellular vaccine are obtainedfrom healthy, unrelated donors. Donors are prescreened to minimize riskfor infectious diseases as described in Example 7, and those that testpositive are eliminated. By using genetically disparate donors, thelikelihood of hyperacute rejection of the second administration isdecreased. The mixed lymphocyte culture is conducted by mixing donor andinactivated patient peripheral blood mononuclear cells at a ratio of10:1, and culturing at 3×10⁶ cells/mL in AIMV supplemented with 2% fetalcalf serum for 3 days at 37° C. The total number of mononuclear cellsrequired for a single inoculum is no more than 1×10⁹. The stimulatedcells are collected and washed by centrifugation, then suspended insterile, injectable saline. Quality control of the production ofactivated cells includes monitoring cell counts and viability, testingfor mycoplasma and endotoxin, and monitoring for lymphocyte activationusing early activation markers, as described in Example 7.

Before use in treatment, the alloactivated cell preparation is alsoevaluated according to functional release criteria. The TetrazoliumReduction Assay (XTT described in Example 3 is conducted on a cellsample. Flow Cytometry is conducted to measure cell surface expressionof CD69 using fluorescent antibody; or increased intracellular esteraseactivity using fluorescein diacetate. Cultured cells are considered tobe sufficiently activated if the level measured in either one (butpreferably both) of these assays is ≧10% above unstimulated donorcontrol value on any day of the culture period (day 1, day 2, or day 3).Once the culture passes the criteria, testing on subsequent days is notneeded. The cells are harvested on day 3, mixed with the requisitenumber of primary or cultured tumor cells, and prepared for humanadministration.

The study is conducted on patients with Stage IV (metastatic) coloncancer. Patents are enrolled in the study under terms of informedconsent, and undergo a standard colectomy. About 1 week later (aroundthe time they are discharged from the hospital), they begin a course offour vaccine injections.

The vaccine composition consists essentially of an alloactivated cellpopulation mixed with tumor cells. Patients receive one of threedifferent doses: 1×10⁸ MLC cells; 3×10⁸ MLC cells; or 1×10⁹ MLC, mixedwith up to 1×10⁷ inactivated tumor cells, depending on availability. Thesame dose is given four times on a weekly schedule.

Initial studies are conducted primarily to determine the maximumtolerated dose (MTD). Undesirable clinical side effects at the injectionsite include an unacceptable level of induration, inflammation, orulceration.

Once the MTD is determined, a comparison is made between the 4-weekvaccination schedule alone, and a vaccination course initiated by directimplantation into a tumor mass. The implant group is treated two days toa week after colectomy, using ultrasound to guide an injection needleinto a sizeable metastatic tumor mass in the liver. The metastatic siteis injected with a preparation of 10×10⁹ MLC alloactivated cells alone,suspended in a minimum volume of saline. Beginning one week later, thepatients in this group also receive the 4-week course of the MLC-tumorcell vaccine.

Safety of the compositions is monitored by several criteria, includinglocal induration, pruritus, or necrosis at the injection site; systemiceffects such as fever, malaise, headache, and altered hematological orrenal parameters.

The presence of a cellular immune response in the treated patient can bemonitored by several criteria. Patient lymphocytes obtained before andafter each inoculation are cultured with irradiated allogeneic cells ofdonor origin or from a third party (for anti-allotype response), orirradiated patient tumor cells, or third-party tumor cells (for specificanti-tumor response). The response of patient lymphocytes in culture isdetermined by measuring proliferation using reduction of MTT or one ofthe other functional assays as a surrogate marker for cellular division.Expression of CD69 is determined by immunofluorocytometry usingPE-labeled antibody.

Optionally, the responding T cells are costained for CD4, CD8, or CD31to identify helper or suppressor subsets, or for CD45RF to distinguishT_(H1) from T_(H2) cells. Cytokines IL-2, IL-4, IFN-γ and TNF-α secretedinto the culture media are quantified by ELISA. IL-2 and IFN-γ correlatewith T_(H1) activity, IL-4 correlates with T_(H2) activity, andTNF-αcorrelates with the activity of both. Patients' PBL are alsooptionally tested for their ability to respond to autologous tumor cellsin culture. General T cell activation can be measured by the functionalassays described in Example 3, [³H] thymidine incorporation, orblastogenesis. Cytotoxic T cell activity can be measured as cytolysis of⁵¹Cr labeled tumor cells. The effective delayed type hypersensitivity(DTH) anti-tumor response in the treated patient is measured bycomparing the 48-hour response of the intradermal administration of5×10⁵ autologous tumor cells, mumps, tricophyton, or PPD antigens withthat observed for the same series before treatment.

The patients are monitored for the extent of the clinical andimmunological response for at least three months following therapy.Clinical criteria is monitored, in part, by tracking the volume of tumormetastasis present in the liver. A CT scan is performed at regularintervals, the volume of each metastatic site is calculated, and thevolumes are compared with the measurements obtained before treatment.Progression of disease is indicated by an increase in volume of themetastasis, or an increase in the number of metastatic sites. Asuccessful outcome is indicated by reversal of the disease, or slowerprogression in comparison with the typical outcome for patents withcolon cancer of the same grade.

Example 8

COMMERCIAL PRODUCTION OF ALLOACTIVATED CELL COMPOSITIONS

This protocol describes the overall approach to production of the mixedlymphocyte culture. The design of this methodology takes into accountGood Manufacturing (GMP) and Good Laboratory (GLP) Practices, andcomplies with requirements of Code 21 of U.S. Federal Regulations.

Patient peripheral blood mononuclear cells, at least 2×10⁹ cells arecollected by modified leukapheresis from the patient to be treated.Isolation of cells is performed on a Baxter Fenwall apheresis machine orequivalent machine using the Stem Cell Collection Procedure. Cells areshipped in a Baxter-type component bag on ice (4-10° C.). Transittemperature is monitored using MONITOR-MARK™ Time/Temperature Tags.

Donor peripheral blood mononuclear cells, at least 10×10⁹ cells, arecollected by modified leukapheresis from a healthy individual. Isolationof cells is performed on a Baxter Fenwall apheresis machine orequivalent ,using the Stem Cell Collection Procedure. Donors areunrelated, anonymous, and random individuals, picked from a list ofprescreened potential donors.

Prescreening of the donors should indicate negative risk factors forHIV, Hepatitis, Spongioform Encephalitides, or Tuberculosis. Each cellcomponent is tested negative for HIV ½ Ab, HIV Ag, CMV Ab, HTLV I/II Ab,HCV Ab, HBcAb, HBsAg and RPR. Cells are shipped in a Baxter-typecomponent bag on ice (4-10° C.).

Upon receipt each component is tested for sterility, appropriate cellcounts, and viability. Components are maintained at 4-10° C. until use,and used or frozen within 72 hours of collection. Thawed frozen materialare used within 2 hours and not re-frozen. Pre-clinical studies indicatethat components stored at 4° C. in ACD anticoagulated plasma or materialfrozen in DMSO-containing media are suitable for the production ofeffective cell compositions.

Plasma is removed form both the donor and patient components bycentrifugation. Donor plasma may be collected and heat-inactivated foruse as a medium supplement. Component cells are suspended in smallvolumes of PBS and appropriate volumes of each suspension is mixed toproduce a culture that contains 3×10⁶ mononuclear cells/ml in AIMVmedium at a ratio of 10:1 to 20:1 (donor:patient cells).Heat-inactivated donor plasma is added to a final concentration of 2%.Mixed cells are pumped into Fenwall 3 liter gas permeable culture bagsthrough the use of the Fenwall solution pump and sterile set-up. Samplesof the component cells may also be set up in small culture tubes fortesting of lymphocyte activation. Testing of functional activity iscompared with control cultures containing unstimulated donor cellsalone.

Cell mixtures are cultured in a ISO-° 9000 Forma 37° C. incubator with5% humidified and HEPA filtered CO₂ for 3 days, and closely monitored.Cells are harvested after culture by centrifugation. Samples are takenfor quality assurance assays. Each preparation is tested for finalsterility, adequate cell counts, adequate viability and functionalactivity.

The cell preparation is suspended in sterile 25% human albumin, andplaced in sterile injectable vials for transport. Each preparation islabeled with an expiration date and time, which is 30 hours afterpackaging, and accompanied by appropriate instructions, releasespecification results, and a MONITOR-MARK™ Time/Temperature Tag. Cellpreparations are packaged and shipped via overnight courier service. Ifnot used immediately, the cells are stored in a refrigerator at 4-10° C.Any preparation not implanted before the expiration date is discarded.

In process tests that measure product consistency include:

pre-screen infectious disease tests;

in process and fmal product sterility tests;

final product mycoplasma and endotoxin;

in process and final product cell counts; in process and final productviability (≧85%).

Cells must also meet satisfactory functional criteria. Preparations notmeeting any of these criteria are not used for treating patients.

TABLE 2 Donor and Patient Screening (At Time Of Leukapheresis Procedure)METHOD (AS PER HOSPITAL BLOOD TEST BANK SOPS) SPECIFICATION Pre-screenfor risk HIV Report Only factors Hepatitis Spongioform encephalitisTuberculosis Adventitious agent HIV 1 and 2 Ab All negative* screeningHIV Ag HBs-Ag HBc Ab* HCV Ab HTLV 1 and 2 Ab CMV Ab* RPR *Patient may bepositive for HBcAb or CMV Ab, and components are labeled as such. If CMVnegative donor components are not available, a CMV Ab positive donorcomponent may be used, even for CMV negative patients.

TABLE 3 Pre-Process Testing Of Donor And Patient Mononuclear Cells (AtTime Of Receipt At Facility, Prior To Irradiation) TEST SPECIFICATIONSterility Sterile Cell Count Patient:  ≧2 × 10⁹ cells Donor: ≧10 × 10⁹cells

TABLE 4 In Process Testing Of Alloactivated Cells TEST ASSAYSPECIFICATION Bioactivity of Tetrazolium Reduction ≧10% abovelymphocytes activation Assay (XTT) unstimulated donor (Tests on days 1,control value on 2, and/or 3 of culture) any day of test Flow Cytometry≧10% above (cell surface expression unstimulated donor of CD69 byfluorescent control value on antibody; or increased any day of testintracellular esterase activity by fluorescein diacetate)

TABLE 5 Final Product Testing TEST SPECIFICATION Sterility Sterile CellCount 9 × 10⁹ cells (± 10%) Viability ≧85% viable cells MycoplasmaNegative (results not available until after the implantation) Endotoxin≦350 EU/total body

Although the foregoing description includes details of some preferredembodiments to facilitate understanding, the skilled practitioner willreadily appreciate that substitutions and modifications may beimplemented without departing from the invention. Examples in thedisclosure should not be construed as limiting the scope of theinvention, which is delineated by the appended claims.

What is claimed as the invention is:
 1. A method for preparing apharmaceutical composition containing alloactivated human donorlymphocytes for treating a tumor in a human patient, comprising thesteps of: a) coculturing the following cells ex vivo: lymphocytes from afirst human donor allogeneic to the patient, and leukocytes from asecond human donor allogeneic to both the first human donor and thepatient, so as to alloactivate the lymphocytes; and b) harvesting thecocultured cells and preparing them for human administration at a timeafter initiation of the coculturing when the harvested cells, uponimplantation in the bed of a solid tumor in the patient, are effectivein treating the solid tumor or eliciting an anti-tumor immunologicalresponse in the patient.
 2. The method according to claim 1, wherein thecocultured cells are harvested at a time when implantation of thecocultured cells elicits a response in the patient against the tumor. 3.The method according to claim 1, wherein the cocultured cells areharvested at a time when a single implantation of the cocultured cellsin the bed of the solid tumor is effective in the treatment of thetumor.
 4. The method according to claim 1, wherein the harvesting instep a) is performed at about the time that at least one of thefollowing criteria is met: i) when the level of secretion of IFN-γ bythe cultured cells is highest; or ii) at about 48 to 72 hours afterinitiation of the culture.
 5. The method according to claim 1, whereinleukocytes from at least two different human donors allogeneic to boththe first human donor and the patient are cocultured in step a).
 6. Themethod according to claim 1, wherein the coculturing of step a) isconducted in a medium containing an H2 receptor antagonist.
 7. Themethod according to claim 6, wherein the H2 receptor antagonist iscimetidine.
 8. The method according to claim 7, wherein the cimetidineis present in the culture medium at a concentration between about 5μg/mL and about 100 μg/mL.
 9. A method for preparing a cultured cellpopulation containing alloactivated human donor lymphocytes effective intreating a tumor in a human patient, comprising the steps of: a)obtaining lymphocytes from a first human donor allogeneic to thepatient, and b) obtaining leukocytes from a second human donorallogeneic to both the first human donor and the patient; c) coculturingthe lymphocytes ex vivo with the leukocytes so as to alloactivate thelymphocytes; d) harvesting the cocultured cells from culture at a timewhen the harvested cells, upon implantation in the bed of a solid tumorin the patient, are effective in treating the tumor or eliciting ananti-tumor immunological response; e) washing culture medium from theharvested cells; and f) verifying that the washed cells are sufficientlysterile for human administration.
 10. The method according to claim 9,incorporating one or more of the following features: i) obtaining atleast about 2×10⁹ peripheral blood mononuclear cells from the firsthuman donor in step a); ii) obtaining at least about 2×10⁸ peripheralblood mononuclear cells from the second human donor in step b); iii)blocking proliferation of the leukocytes prior to step c); iv)coculturing the donor lymphocytes with the patient leukocytes at a ratioof about 5:1 to 20:1 in step c); or v) producing at least about 2×10⁹cocultured cells suitable for human administration after completion ofstep f).
 11. A pharmaceutical composition prepared according to themethod of claim 1, which, upon implantation at or around the site of asolid tumor in said human patient with or without partial resection ofthe tumor, is effective in eliciting an anti-tumor immunologicalresponse.
 12. A pharmaceutical composition prepared according to themethod of claim 1, which, upon implantation at or around the site of asolid tumor in a human patient with or without partial resection of thetumor, is effective in the treatment of the tumor.
 13. Thepharmaceutical composition of claim 11 having one or more of thefollowing features: i) containing between about 2×10⁹ and 2×10¹⁰cultured peripheral blood mononuclear cells originating from the firstdonor; ii) containing between about 1×10⁸ and 2×10⁹ cultured peripheralblood mononuclear cells originating from the second donor; iii) beingsubstantially free of any exogenously added lymphocyte proliferationagent; iv) containing a physiologically compatible carrier selected fromthe group consisting of physiological saline, buffered medium, andclotted plasma.
 14. The pharmaceutical composition of claim 11, whereina single implantation of the cocultured cells is effective in elicitingan anti-tumor immunological response.
 15. A method of eliciting ananti-tumor immunological response in a human patient, comprisingimplanting in or around the bed of a solid tumor in the patient apharmaceutical composition according to claim
 10. 16. A method oftreating a tumor in a human patient, comprising implanting in or aroundthe bed of a solid tumor in the patient a pharmaceutical compositionaccording to claim
 12. 17. The method according to claim 14, furthercomprising the additional step of administering to the patient at a sitedistant from the tumor a second composition comprising alloactivatedhuman lymphocytes allogeneic to the patient mixed with inactivated tumorcells from the patient or inactivated progeny of such tumor cells. 18.The method according to claim 15, wherein the tumor is a malignancyselected from the group consisting of melanoma, pancreatic cancer, livercancer, colon cancer, prostate cancer, and breast cancer.